RareBench/RAMEDIS.jsonl

{"Phenotype": ["HP:0001522", "HP:0001942", "HP:0003210", "HP:0003819"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001270", "HP:0001290", "HP:0001522", "HP:0002090", "HP:0040156"], "RareDisease": ["OMIM:271980", "ORPHA:22"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000776", "HP:0001270", "HP:0001272", "HP:0001508", "HP:0001522", "HP:0002036", "HP:0009125", "HP:0011804", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000126", "HP:0000750", "HP:0001197", "HP:0001249", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001945", "HP:0002179", "HP:0002305", "HP:0002751", "HP:0003811", "HP:0003819", "HP:0010910", "HP:0010911", "HP:0010913", "HP:0011421", "HP:0011968", "HP:0040156"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0000988", "HP:0001197", "HP:0001513", "HP:0001522", "HP:0002014", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004429", "HP:0004923", "HP:0025474", "HP:0025475", "HP:0030350", "HP:0100790"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000976", "HP:0000988", "HP:0001522", "HP:0001596", "HP:0002151", "HP:0002490"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000510", "HP:0001249", "HP:0001272", "HP:0001522", "HP:0001907", "HP:0001999", "HP:0002683", "HP:0009125", "HP:0012642", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000476", "HP:0001254", "HP:0001290", "HP:0001332", "HP:0001522", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0002094", "HP:0002329", "HP:0002360", "HP:0003150", "HP:0003811", "HP:0008315", "HP:0100660"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001254", "HP:0001522", "HP:0001987", "HP:0002329", "HP:0002360", "HP:0003811", "HP:0003819", "HP:0010895", "HP:0010967", "HP:0011968"], "RareDisease": ["OMIM:243500", "ORPHA:33", "CCRD:58"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000486", "HP:0000639", "HP:0001249", "HP:0001251", "HP:0001265", "HP:0001270", "HP:0001272", "HP:0001290", "HP:0001298", "HP:0001510", "HP:0001522", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000639", "HP:0000648", "HP:0001197", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001629", "HP:0001987", "HP:0002160", "HP:0003348", "HP:0003811", "HP:0003819", "HP:0010967", "HP:0012120", "HP:0040156"], "RareDisease": ["OMIM:277400", "ORPHA:79282", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001943", "HP:0002013", "HP:0002014", "HP:0002910", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001259", "HP:0001522", "HP:0002153", "HP:0002902", "HP:0003811", "HP:0005972", "HP:0040156"], "RareDisease": ["OMIM:271980", "ORPHA:22"], "Department": null}
{"Phenotype": ["HP:0000508", "HP:0001083", "HP:0001176", "HP:0001249", "HP:0001270", "HP:0001833", "HP:0002160", "HP:0003235", "HP:0003819", "HP:0011421", "HP:0012378"], "RareDisease": ["OMIM:236200", "ORPHA:394", "CCRD:45"], "Department": null}
{"Phenotype": ["HP:0000154", "HP:0000286", "HP:0000670", "HP:0000842", "HP:0008070", "HP:0001250", "HP:0001522", "HP:0001943", "HP:0003811", "HP:0003819", "HP:0011902", "HP:0011968"], "RareDisease": ["OMIM:601820", "CCRD:20"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001522", "HP:0001903", "HP:0001987", "HP:0002154", "HP:0002240", "HP:0003811", "HP:0003819", "HP:0010967", "HP:0012277"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0001873", "HP:0001882", "HP:0001942", "HP:0002104", "HP:0003210", "HP:0003811", "HP:0011968", "HP:0012120", "HP:0012638"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001259", "HP:0001522", "HP:0001699", "HP:0001943", "HP:0002013", "HP:0003155", "HP:0008315", "HP:0010899", "HP:0010916", "HP:0025435"], "RareDisease": ["OMIM:212140", "ORPHA:158", "CCRD:15"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001522", "HP:0002312", "HP:0002329", "HP:0002360", "HP:0002370", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0011968"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000821", "HP:0001260", "HP:0001264", "HP:0001298", "HP:0001347", "HP:0002510", "HP:0003219", "HP:0003688", "HP:0004429", "HP:0010895", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:220110"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000476", "HP:0000975", "HP:0001254", "HP:0001290", "HP:0001332", "HP:0001522", "HP:0001942", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0002094", "HP:0002329", "HP:0002360", "HP:0003150", "HP:0003530", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0100660"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001249", "HP:0001347", "HP:0001522", "HP:0002355", "HP:0002500", "HP:0003551", "HP:0003819", "HP:0009046"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001257", "HP:0001290", "HP:0001513", "HP:0001522", "HP:0001943", "HP:0003811", "HP:0010910", "HP:0010911", "HP:0010913", "HP:0100613"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001513", "HP:0001522", "HP:0003348", "HP:0003355", "HP:0003573", "HP:0004342", "HP:0010899", "HP:0010917", "HP:0011421", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001942", "HP:0001945", "HP:0001987", "HP:0002013", "HP:0003215", "HP:0003344", "HP:0010895", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0000952", "HP:0001290", "HP:0001903", "HP:0002160", "HP:0002344", "HP:0003658", "HP:0003819", "HP:0004429", "HP:0010472", "HP:0012335"], "RareDisease": ["OMIM:236200", "ORPHA:394", "CCRD:45"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0002781", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0006510", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001250", "HP:0001257", "HP:0001522", "HP:0001596", "HP:0002094", "HP:0012378", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001513", "HP:0001522", "HP:0001945", "HP:0002013", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000988", "HP:0001522", "HP:0001596", "HP:0001942", "HP:0002490", "HP:0003355", "HP:0010895", "HP:0025474", "HP:0025475", "HP:0030350", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001944", "HP:0003210", "HP:0003811", "HP:0011968"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0001945", "HP:0002151", "HP:0002329", "HP:0002360", "HP:0003209", "HP:0003353", "HP:0003355", "HP:0010280", "HP:0010307", "HP:0010895", "HP:0012378", "HP:0040156", "HP:0100758"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003215", "HP:0003344", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0000670", "HP:0001513", "HP:0002910", "HP:0003819", "HP:0010472", "HP:0010837", "HP:0010839", "HP:0010899", "HP:0010916", "HP:0011967", "HP:0040303"], "RareDisease": ["OMIM:277900", "ORPHA:905", "CCRD:37"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003231", "HP:0003819", "HP:0004429", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0003355", "HP:0010895", "HP:0010967", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0002240", "HP:0002789", "HP:0003535", "HP:0003811", "HP:0011968"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000975", "HP:0001197", "HP:0001254", "HP:0001270", "HP:0001513", "HP:0001522", "HP:0001943", "HP:0001950", "HP:0001987", "HP:0002045", "HP:0002329", "HP:0002360", "HP:0002789", "HP:0003218", "HP:0003811", "HP:0003819", "HP:0011966", "HP:0200039", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000649", "HP:0000737", "HP:0001250", "HP:0001290", "HP:0001522", "HP:0002305", "HP:0003150", "HP:0003811"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0003161", "HP:0003163", "HP:0003231", "HP:0003819", "HP:0010893"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001513", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000752", "HP:0001249", "HP:0001250", "HP:0001513", "HP:0003231", "HP:0003510", "HP:0003819", "HP:0004923", "HP:0011421", "HP:0040156", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001290", "HP:0001522", "HP:0001873", "HP:0001882", "HP:0001942", "HP:0001987", "HP:0002013", "HP:0002912", "HP:0003811", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001942", "HP:0001987", "HP:0002013", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0001987", "HP:0002181", "HP:0003218", "HP:0003811"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001290", "HP:0001510", "HP:0001522", "HP:0001596", "HP:0002380", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001513", "HP:0003124", "HP:0003231", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000047", "HP:0001522", "HP:0001622", "HP:0003231", "HP:0003510", "HP:0003811", "HP:0004923", "HP:0100790"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000369", "HP:0000431", "HP:0000486", "HP:0000750", "HP:0001159", "HP:0001249", "HP:0001270", "HP:0001522", "HP:0002355", "HP:0003462", "HP:0003510", "HP:0003551", "HP:0003811", "HP:0003819", "HP:0009046", "HP:0010569", "HP:0012714"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001522", "HP:0001944", "HP:0001945", "HP:0002014", "HP:0002179", "HP:0002305", "HP:0002344", "HP:0003150", "HP:0003530", "HP:0003819", "HP:0008315", "HP:0012071"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001270", "HP:0001290", "HP:0001385", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000278", "HP:0001197", "HP:0001250", "HP:0001290", "HP:0001522", "HP:0002104", "HP:0002179", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000729", "HP:0000742", "HP:0000752", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001513", "HP:0001522", "HP:0003155", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0006254", "HP:0010899", "HP:0010916", "HP:0040303"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0002013", "HP:0003573", "HP:0003811", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923", "HP:0010917"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001513", "HP:0003819", "HP:0010967", "HP:0011421"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001249", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000047", "HP:0000252", "HP:0000369", "HP:0000486", "HP:0000508", "HP:0000540", "HP:0000976", "HP:0000988", "HP:0001159", "HP:0001249", "HP:0001254", "HP:0001270", "HP:0001290", "HP:0001332", "HP:0001522", "HP:0002013", "HP:0002019", "HP:0002329", "HP:0002360", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0010569", "HP:0011968", "HP:0012418", "HP:0012714"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001265", "HP:0001290", "HP:0001513", "HP:0001522", "HP:0001945", "HP:0002059", "HP:0010899"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0001513", "HP:0001522", "HP:0001680", "HP:0001945", "HP:0002090", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0002160", "HP:0003235", "HP:0003355", "HP:0003811", "HP:0003819"], "RareDisease": ["OMIM:236200", "ORPHA:394", "CCRD:45"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001290", "HP:0003819", "HP:0004353", "HP:0012127"], "RareDisease": ["OMIM:274270"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0002093", "HP:0003811", "HP:0004353", "HP:0012127"], "RareDisease": ["OMIM:274270"], "Department": null}
{"Phenotype": ["HP:0000980", "HP:0001522", "HP:0001541", "HP:0001894", "HP:0001903", "HP:0003073", "HP:0003075", "HP:0003155", "HP:0003231", "HP:0003355", "HP:0006254", "HP:0010472", "HP:0100790"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001270", "HP:0001522", "HP:0010899"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0002027", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004429", "HP:0010895", "HP:0010967", "HP:0011421", "HP:0500001"], "RareDisease": ["OMIM:243500", "ORPHA:33", "CCRD:58"], "Department": null}
{"Phenotype": ["HP:0000822", "HP:0001249", "HP:0001513", "HP:0003231", "HP:0004923", "HP:0011421", "HP:0040156", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001518", "HP:0001522", "HP:0003348", "HP:0003811", "HP:0003819", "HP:0010967", "HP:0012714"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001522", "HP:0002329", "HP:0002360", "HP:0003218", "HP:0012025"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001332", "HP:0002060", "HP:0003150", "HP:0003819", "HP:0008315", "HP:0012447"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0001259", "HP:0001290", "HP:0001298", "HP:0001638", "HP:0001903", "HP:0001943", "HP:0002013", "HP:0002240", "HP:0002910", "HP:0003819", "HP:0008315", "HP:0010472", "HP:0010899", "HP:0010916"], "RareDisease": ["OMIM:212140", "ORPHA:158", "CCRD:15"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000639", "HP:0001251", "HP:0001265", "HP:0001270", "HP:0001272", "HP:0001290", "HP:0001298", "HP:0001510", "HP:0001522", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000545", "HP:0000750", "HP:0001083", "HP:0001249", "HP:0001522", "HP:0002160", "HP:0003235", "HP:0003355", "HP:0003819", "HP:0010916", "HP:0100660"], "RareDisease": ["OMIM:236200", "ORPHA:394", "CCRD:45"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001251", "HP:0001254", "HP:0001347", "HP:0001942", "HP:0001945", "HP:0001987", "HP:0002014", "HP:0002329", "HP:0002360", "HP:0002380", "HP:0003218", "HP:0003819", "HP:0011421"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000307", "HP:0000331", "HP:0000486", "HP:0000508", "HP:0000752", "HP:0001159", "HP:0001249", "HP:0001251", "HP:0001290", "HP:0001347", "HP:0001508", "HP:0001522", "HP:0003146", "HP:0003462", "HP:0003819", "HP:0010569", "HP:0011968", "HP:0012378"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0002151", "HP:0002155", "HP:0002240", "HP:0003811", "HP:0010899", "HP:0010916", "HP:0025435", "HP:0040081"], "RareDisease": ["OMIM:232400", "ORPHA:366"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0001290", "HP:0001522", "HP:0002120", "HP:0002305", "HP:0003150", "HP:0003811", "HP:0008315", "HP:0011421", "HP:0012071"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001987", "HP:0002013", "HP:0002154", "HP:0003108", "HP:0003348", "HP:0003819", "HP:0008064", "HP:0010903", "HP:0010967", "HP:0040156"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001270", "HP:0001999", "HP:0002683", "HP:0003819", "HP:0010996", "HP:0040156"], "RareDisease": ["OMIM:271980", "ORPHA:22"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001249", "HP:0001270", "HP:0001399", "HP:0001522", "HP:0001622", "HP:0002014", "HP:0003573", "HP:0003645", "HP:0003811", "HP:0003819", "HP:0004342", "HP:0010899", "HP:0010916", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001987", "HP:0003355", "HP:0003811", "HP:0003819", "HP:0010907", "HP:0011966"], "RareDisease": ["OMIM:605814", "ORPHA:247598", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001945", "HP:0003231", "HP:0003819", "HP:0004429", "HP:0004923", "HP:0010472", "HP:0011421", "HP:0012343", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001290", "HP:0001337", "HP:0001522", "HP:0002179", "HP:0002329", "HP:0002360", "HP:0003811", "HP:0004357", "HP:0040156", "HP:0500001"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0001622", "HP:0001903", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0012343", "HP:0031437", "HP:0040303", "HP:0100511"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000316", "HP:0000463", "HP:0000742", "HP:0000750", "HP:0000752", "HP:0001159", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001522", "HP:0001760", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0003819", "HP:0010569", "HP:0012714"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000750", "HP:0001197", "HP:0001249", "HP:0001270", "HP:0001290", "HP:0001508", "HP:0001518", "HP:0001522", "HP:0001744", "HP:0001903", "HP:0001919", "HP:0001942", "HP:0001943", "HP:0001944", "HP:0001945", "HP:0001987", "HP:0002045", "HP:0002090", "HP:0002149", "HP:0002151", "HP:0002154", "HP:0002240", "HP:0002912", "HP:0003108", "HP:0003138", "HP:0003155", "HP:0003210", "HP:0003259", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0008315", "HP:0010472", "HP:0010899", "HP:0010916", "HP:0010919", "HP:0011227", "HP:0011968", "HP:0012120", "HP:0012622", "HP:0040156"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001254", "HP:0001290", "HP:0001522", "HP:0002329", "HP:0002360", "HP:0004353", "HP:0012127"], "RareDisease": ["OMIM:274270"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001987", "HP:0003811", "HP:0003819", "HP:0010895", "HP:0010967"], "RareDisease": ["OMIM:243500", "ORPHA:33", "CCRD:58"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001290", "HP:0001522", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001264", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0002094", "HP:0002104", "HP:0002179", "HP:0002510", "HP:0003811", "HP:0010910", "HP:0010911", "HP:0010913", "HP:0011968", "HP:0500001"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0000709", "HP:0000939", "HP:0001249", "HP:0001903", "HP:0001987", "HP:0002059", "HP:0002154", "HP:0002751", "HP:0003138", "HP:0003259", "HP:0003348", "HP:0003510", "HP:0010472", "HP:0010967", "HP:0011421", "HP:0012714", "HP:0040156", "HP:0100613", "HP:0500001"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001250", "HP:0001251", "HP:0001337", "HP:0003819", "HP:0040144"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0001270", "HP:0001522", "HP:0010899"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001987", "HP:0003573", "HP:0003811", "HP:0011966"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001522", "HP:0001942", "HP:0001943", "HP:0001987", "HP:0002013", "HP:0002014", "HP:0002240", "HP:0002329", "HP:0002360", "HP:0003215", "HP:0003344", "HP:0003819", "HP:0004429", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0001744", "HP:0002093"], "RareDisease": ["OMIM:220100", "ORPHA:214"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001987", "HP:0002013", "HP:0003075", "HP:0003138", "HP:0003354", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0010910", "HP:0010912", "HP:0010967", "HP:0011968", "HP:0012101", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003231", "HP:0003819", "HP:0004429", "HP:0004923", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001197", "HP:0001249", "HP:0001513", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001892", "HP:0001987", "HP:0002013", "HP:0003218", "HP:0003256"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001290", "HP:0001347", "HP:0001987", "HP:0002060", "HP:0003819", "HP:0012447", "HP:0040147"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001251", "HP:0001272", "HP:0001522", "HP:0001907", "HP:0002401", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001622", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001249", "HP:0001250", "HP:0001254", "HP:0001270", "HP:0001290", "HP:0001337", "HP:0001522", "HP:0001882", "HP:0001945", "HP:0001987", "HP:0002013", "HP:0002020", "HP:0002090", "HP:0002151", "HP:0002154", "HP:0002329", "HP:0002355", "HP:0002360", "HP:0002789", "HP:0003138", "HP:0003231", "HP:0003348", "HP:0003551", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0008358", "HP:0009046", "HP:0010280", "HP:0010910", "HP:0010967", "HP:0012277", "HP:0012714"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0001959", "HP:0002910", "HP:0010837", "HP:0011421", "HP:0011967"], "RareDisease": ["OMIM:277900", "ORPHA:905", "CCRD:37"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001254", "HP:0001290", "HP:0001522", "HP:0002013", "HP:0002329", "HP:0002360", "HP:0003217", "HP:0003218", "HP:0003811"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000750", "HP:0001197", "HP:0001249", "HP:0001270", "HP:0001290", "HP:0001513", "HP:0001522", "HP:0001903", "HP:0003155", "HP:0003811", "HP:0003819", "HP:0004342", "HP:0010472", "HP:0011968", "HP:0012024", "HP:0012343", "HP:0040303"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001513", "HP:0001760", "HP:0001987", "HP:0003819"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000752", "HP:0001522", "HP:0010899", "HP:0011968", "HP:0012447"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000123", "HP:0001290", "HP:0001522", "HP:0001629", "HP:0001638", "HP:0001642"], "RareDisease": ["OMIM:261750"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0001257", "HP:0001347", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001290", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001298", "HP:0001522", "HP:0002179", "HP:0003150", "HP:0003530", "HP:0003819", "HP:0008315", "HP:0040156"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000639", "HP:0000752", "HP:0000961", "HP:0000969", "HP:0001249", "HP:0001250", "HP:0001264", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0002014", "HP:0002090", "HP:0002094", "HP:0002153", "HP:0002179", "HP:0002240", "HP:0002286", "HP:0002510", "HP:0002901", "HP:0003811", "HP:0010307", "HP:0011364", "HP:0012714"], "RareDisease": ["OMIM:266130"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001249", "HP:0001251", "HP:0001270", "HP:0001272", "HP:0001290", "HP:0001394", "HP:0001395", "HP:0001522", "HP:0001907", "HP:0001976", "HP:0003819", "HP:0009125", "HP:0011421", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0001250", "HP:0001290", "HP:0001347", "HP:0001522", "HP:0002179", "HP:0010899", "HP:0011968"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004386", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001259", "HP:0001315", "HP:0001596", "HP:0001942", "HP:0002181", "HP:0002500", "HP:0003819", "HP:0004429", "HP:0010911", "HP:0011421"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0002027", "HP:0003163", "HP:0003819"], "RareDisease": ["OMIM:176000", "ORPHA:79276", "CCRD:92"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0001942", "HP:0003811", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001254", "HP:0001290", "HP:0001510", "HP:0002329", "HP:0002360", "HP:0003819", "HP:0040319"], "RareDisease": ["OMIM:203500", "ORPHA:56"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0003355", "HP:0003811", "HP:0004357", "HP:0010912", "HP:0010914"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001640", "HP:0001943", "HP:0002151", "HP:0002240", "HP:0002789", "HP:0003215", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0010967"], "RareDisease": ["OMIM:201475", "ORPHA:26793", "CCRD:116"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001254", "HP:0001522", "HP:0001942", "HP:0001943", "HP:0001945", "HP:0002013", "HP:0002329", "HP:0002344", "HP:0002360", "HP:0003150", "HP:0003344", "HP:0003819", "HP:0004429", "HP:0010895", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0001943", "HP:0003076", "HP:0010472"], "RareDisease": ["OMIM:125850", "ORPHA:552"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000238", "HP:0000256", "HP:0000975", "HP:0001250", "HP:0001254", "HP:0001332", "HP:0001347", "HP:0001522", "HP:0001903", "HP:0001945", "HP:0002013", "HP:0002059", "HP:0002179", "HP:0002329", "HP:0002360", "HP:0002380", "HP:0002781", "HP:0002922", "HP:0003150", "HP:0003819", "HP:0004429", "HP:0006510", "HP:0011421"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0004923", "HP:0100602", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0040156", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000988", "HP:0001254", "HP:0001290", "HP:0001522", "HP:0001744", "HP:0001945", "HP:0002013", "HP:0002090", "HP:0002240", "HP:0002329", "HP:0002360", "HP:0003108", "HP:0003131", "HP:0003218", "HP:0003532", "HP:0003819", "HP:0010916", "HP:0011968", "HP:0025474", "HP:0025475", "HP:0030350"], "RareDisease": ["OMIM:258900", "ORPHA:30"], "Department": null}
{"Phenotype": ["HP:0000961", "HP:0000976", "HP:0000988", "HP:0001290", "HP:0001522", "HP:0001903", "HP:0001942", "HP:0001987", "HP:0002014", "HP:0002789", "HP:0003209", "HP:0003353", "HP:0003355", "HP:0003811", "HP:0010895", "HP:0010996", "HP:0040156"], "RareDisease": ["OMIM:253270", "ORPHA:79242", "CCRD:44"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001251", "HP:0001254", "HP:0001987", "HP:0002013", "HP:0002329", "HP:0002360", "HP:0003218", "HP:0011421"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0002013", "HP:0003219", "HP:0003819", "HP:0010967", "HP:0011421", "HP:0100950"], "RareDisease": ["OMIM:201470"], "Department": null}
{"Phenotype": ["HP:0000369", "HP:0000431", "HP:0000463", "HP:0000508", "HP:0001159", "HP:0001249", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0010569", "HP:0011968"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001251", "HP:0001337", "HP:0001522", "HP:0002059", "HP:0002134", "HP:0003811", "HP:0003819", "HP:0040144"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0001250", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0002179", "HP:0003215", "HP:0003535", "HP:0003811", "HP:0003819", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0000976", "HP:0000988", "HP:0001250", "HP:0001522", "HP:0001945", "HP:0011227", "HP:0040144", "HP:0040303"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0000123", "HP:0001522", "HP:0002148", "HP:0002813", "HP:0003117", "HP:0003155", "HP:0003819"], "RareDisease": ["OMIM:307800", "ORPHA:89936", "CCRD:51"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000976", "HP:0000988", "HP:0001522", "HP:0001882", "HP:0001987", "HP:0002154", "HP:0003108", "HP:0003155", "HP:0003819", "HP:0010899", "HP:0010916", "HP:0010967", "HP:0011421", "HP:0012278", "HP:0040156"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001290", "HP:0001522", "HP:0002160", "HP:0002500", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0008315", "HP:0012120"], "RareDisease": ["OMIM:277400", "ORPHA:79282", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003811", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001257", "HP:0001290", "HP:0001347", "HP:0001522", "HP:0001987", "HP:0002329", "HP:0002360", "HP:0003811", "HP:0011968"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001942", "HP:0003210", "HP:0003819"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000752", "HP:0001257", "HP:0001522", "HP:0001878", "HP:0001942", "HP:0003573", "HP:0003811", "HP:0004429", "HP:0010472", "HP:0025435"], "RareDisease": ["OMIM:266130"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001622", "HP:0001987", "HP:0002098", "HP:0002104", "HP:0003811", "HP:0005972", "HP:0011966", "HP:0012418"], "RareDisease": ["OMIM:605814", "ORPHA:247598", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000729", "HP:0000822", "HP:0000969", "HP:0001249", "HP:0001250", "HP:0001259", "HP:0001290", "HP:0001522", "HP:0001733", "HP:0001882", "HP:0001903", "HP:0001919", "HP:0001987", "HP:0001997", "HP:0002013", "HP:0002149", "HP:0002151", "HP:0002154", "HP:0002312", "HP:0002370", "HP:0002751", "HP:0002902", "HP:0002912", "HP:0003075", "HP:0003097", "HP:0003138", "HP:0003155", "HP:0003210", "HP:0003259", "HP:0003281", "HP:0003819", "HP:0010472", "HP:0010899", "HP:0010914", "HP:0010916", "HP:0010967", "HP:0011421", "HP:0012120", "HP:0012239", "HP:0012622", "HP:0100613"], "RareDisease": ["OMIM:251110", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000639", "HP:0001197", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001596", "HP:0002059", "HP:0002500", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261630", "ORPHA:226", "CCRD:49"], "Department": null}
{"Phenotype": ["HP:0000988", "HP:0001522", "HP:0003076", "HP:0003219", "HP:0003688", "HP:0010895", "HP:0011968", "HP:0012719", "HP:0025474", "HP:0025475", "HP:0030350"], "RareDisease": ["OMIM:220110"], "Department": null}
{"Phenotype": ["HP:0000961", "HP:0001250", "HP:0001522", "HP:0001987", "HP:0002181", "HP:0002380", "HP:0003218", "HP:0003572", "HP:0003811", "HP:0005961"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0000988", "HP:0001250", "HP:0001522", "HP:0001987", "HP:0003355", "HP:0003811", "HP:0010895", "HP:0010899", "HP:0025474", "HP:0025475", "HP:0030350"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0002093", "HP:0002179", "HP:0003811", "HP:0010910", "HP:0010911", "HP:0010913", "HP:0011968", "HP:0100806"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001513", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0010967", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001250", "HP:0001270", "HP:0001522", "HP:0002500", "HP:0003231", "HP:0003819", "HP:0004923", "HP:0100613", "HP:0100660"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001744", "HP:0002240", "HP:0002910", "HP:0003819", "HP:0010837", "HP:0010839", "HP:0010899", "HP:0010916", "HP:0011421", "HP:0011967", "HP:0025321"], "RareDisease": ["OMIM:277900", "ORPHA:905", "CCRD:37"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001249", "HP:0001251", "HP:0001272", "HP:0001290", "HP:0001522", "HP:0001999", "HP:0002683", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0001290", "HP:0001522", "HP:0002060", "HP:0002151", "HP:0003072", "HP:0003150", "HP:0010908", "HP:0010967"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0001197", "HP:0001518", "HP:0001522", "HP:0001698", "HP:0002202", "HP:0003231", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011968"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001987", "HP:0002013", "HP:0003217", "HP:0003218", "HP:0003819"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001513", "HP:0001522", "HP:0003811", "HP:0004923", "HP:0010917", "HP:0040156", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000105", "HP:0000508", "HP:0000613", "HP:0001254", "HP:0001259", "HP:0001290", "HP:0001522", "HP:0001635", "HP:0001738", "HP:0001873", "HP:0001875", "HP:0001903", "HP:0001919", "HP:0001943", "HP:0001994", "HP:0002013", "HP:0002151", "HP:0002329", "HP:0002360", "HP:0003344", "HP:0003542", "HP:0003811", "HP:0003819", "HP:0004322", "HP:0004429", "HP:0008315", "HP:0010996", "HP:0011355", "HP:0011968", "HP:0012622", "HP:0040155"], "RareDisease": ["OMIM:557000", "ORPHA:699", "CCRD:72.7"], "Department": null}
{"Phenotype": ["HP:0000289", "HP:0000343", "HP:0000463", "HP:0001159", "HP:0001290", "HP:0001522", "HP:0002002", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0010569", "HP:0011968"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0002013", "HP:0002027", "HP:0003819", "HP:0004429"], "RareDisease": ["OMIM:176000", "ORPHA:79276", "CCRD:92"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001942", "HP:0001987", "HP:0003108", "HP:0003217", "HP:0003268", "HP:0003811", "HP:0010909", "HP:0011966"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001254", "HP:0001290", "HP:0001522", "HP:0001944", "HP:0001987", "HP:0002160", "HP:0002329", "HP:0002360", "HP:0002912", "HP:0008315", "HP:0012120"], "RareDisease": ["OMIM:251110", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000752", "HP:0001290", "HP:0001522", "HP:0001622", "HP:0001987", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0010899", "HP:0010916", "HP:0040081"], "RareDisease": ["OMIM:201475", "ORPHA:26793", "CCRD:116"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0002781", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0006510"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001257", "HP:0001522", "HP:0001622", "HP:0002595", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0012343", "HP:0012418", "HP:0030995", "HP:0040126", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003231", "HP:0003819", "HP:0004429", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003355", "HP:0010895", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000752", "HP:0001250", "HP:0001251", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0003819", "HP:0040156"], "RareDisease": ["OMIM:271980", "ORPHA:22"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001649", "HP:0001942", "HP:0002013", "HP:0002240", "HP:0002789", "HP:0003811"], "RareDisease": ["OMIM:207900", "ORPHA:23"], "Department": null}
{"Phenotype": ["HP:0000618", "HP:0001903", "HP:0001987", "HP:0002024", "HP:0002154", "HP:0002315", "HP:0003510", "HP:0003819", "HP:0005961", "HP:0011421", "HP:0011968", "HP:0012026", "HP:0012278", "HP:0100613"], "RareDisease": ["OMIM:258870", "ORPHA:414"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001290", "HP:0001522", "HP:0001987", "HP:0002181", "HP:0003811", "HP:0011968"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0000618", "HP:0000639", "HP:0001250", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0002179", "HP:0003811", "HP:0010899", "HP:0012447", "HP:0012714"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0000238", "HP:0000252", "HP:0000486", "HP:0000639", "HP:0001249", "HP:0001522", "HP:0001622", "HP:0002093", "HP:0002160", "HP:0003811", "HP:0003819", "HP:0010967", "HP:0012120", "HP:0100660"], "RareDisease": ["OMIM:277400", "ORPHA:79282", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0002013", "HP:0003811", "HP:0004386", "HP:0010967", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0001882", "HP:0001942", "HP:0001987", "HP:0003811"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000491", "HP:0000509", "HP:0000613", "HP:0000962", "HP:0001249", "HP:0001250", "HP:0003231", "HP:0003819", "HP:0009926"], "RareDisease": ["OMIM:276600", "ORPHA:28378"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923", "HP:0010917", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000961", "HP:0001250", "HP:0001522", "HP:0001987", "HP:0003811", "HP:0008160"], "RareDisease": ["OMIM:232200", "CCRD:35.1"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0002013", "HP:0040319"], "RareDisease": ["OMIM:203500", "ORPHA:56"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001254", "HP:0001510", "HP:0001522", "HP:0001942", "HP:0001987", "HP:0002329", "HP:0002360", "HP:0010910", "HP:0010911", "HP:0010913", "HP:0011968", "HP:0012714", "HP:0040156"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0000976", "HP:0000988", "HP:0001259", "HP:0001290", "HP:0001522", "HP:0001943", "HP:0001945", "HP:0001987", "HP:0002013", "HP:0002181", "HP:0002305", "HP:0003217", "HP:0003218", "HP:0003355", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004429", "HP:0010907", "HP:0010909", "HP:0011421", "HP:0011966", "HP:0012127", "HP:0012819", "HP:0040081"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0001249", "HP:0001254", "HP:0001522", "HP:0001662", "HP:0001987", "HP:0002104", "HP:0002181", "HP:0002329", "HP:0002360", "HP:0002615", "HP:0003217", "HP:0003572", "HP:0003811", "HP:0004429"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001249", "HP:0001251", "HP:0001270", "HP:0001272", "HP:0001513", "HP:0001522", "HP:0001907", "HP:0003819", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0100790"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001272", "HP:0001508", "HP:0001522", "HP:0001907", "HP:0003811", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001522", "HP:0001942", "HP:0001943", "HP:0001987", "HP:0002013", "HP:0002090", "HP:0002240", "HP:0003215", "HP:0003535", "HP:0008315", "HP:0010895", "HP:0012071", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001259", "HP:0001290", "HP:0001522", "HP:0001873", "HP:0001903", "HP:0002013", "HP:0002094", "HP:0002329", "HP:0002360", "HP:0002901", "HP:0003811", "HP:0004360", "HP:0010472", "HP:0010895", "HP:0011968", "HP:0040156"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001251", "HP:0001272", "HP:0001522", "HP:0001907", "HP:0003819", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001987", "HP:0003218", "HP:0003811"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000750", "HP:0001159", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001290", "HP:0001508", "HP:0001522", "HP:0001622", "HP:0001903", "HP:0001999", "HP:0002179", "HP:0002683", "HP:0003811", "HP:0003819", "HP:0004342", "HP:0010472", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001254", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0002329", "HP:0002360", "HP:0003150"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000842", "HP:0001197", "HP:0001522", "HP:0001943", "HP:0003161", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0006254"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0001257", "HP:0001265", "HP:0001290", "HP:0001522", "HP:0003811", "HP:0040081", "HP:0040301"], "RareDisease": ["OMIM:307030", "ORPHA:408"], "Department": null}
{"Phenotype": ["HP:0000510", "HP:0000602", "HP:0000649", "HP:0001249", "HP:0001251", "HP:0001270", "HP:0001272", "HP:0001290", "HP:0001522", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001638", "HP:0001945", "HP:0003110", "HP:0003819", "HP:0004386", "HP:0008315"], "RareDisease": ["OMIM:212140", "ORPHA:158", "CCRD:15"], "Department": null}
{"Phenotype": ["HP:0000570", "HP:0001254", "HP:0001257", "HP:0001522", "HP:0001662", "HP:0001987", "HP:0002013", "HP:0002104", "HP:0002329", "HP:0002360", "HP:0003217", "HP:0003218", "HP:0003572", "HP:0003811"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001942", "HP:0003210"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000047", "HP:0000252", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0010569", "HP:0011968"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000975", "HP:0001522", "HP:0001638", "HP:0001640", "HP:0002615", "HP:0002789", "HP:0003355", "HP:0003819", "HP:0010895", "HP:0011968", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0000976", "HP:0000988", "HP:0001197", "HP:0001290", "HP:0001522", "HP:0002151", "HP:0003811", "HP:0003819"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0003124", "HP:0003231", "HP:0003355", "HP:0004923", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000123", "HP:0001279", "HP:0001522", "HP:0001622", "HP:0002013", "HP:0002014", "HP:0002910", "HP:0003811", "HP:0003819"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000822", "HP:0000867", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001638", "HP:0001903", "HP:0001919", "HP:0001987", "HP:0002013", "HP:0002149", "HP:0002154", "HP:0002789", "HP:0002912", "HP:0003138", "HP:0003210", "HP:0003259", "HP:0003348", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0008315", "HP:0010472", "HP:0011421", "HP:0011968", "HP:0012120", "HP:0012622"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001254", "HP:0001284", "HP:0001290", "HP:0001332", "HP:0001522", "HP:0001945", "HP:0002094", "HP:0002154", "HP:0002179", "HP:0002329", "HP:0002360", "HP:0002380", "HP:0003150", "HP:0003217", "HP:0003530", "HP:0010967", "HP:0011968"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001522", "HP:0001945", "HP:0001987", "HP:0002329", "HP:0002360", "HP:0003218", "HP:0003811", "HP:0004429", "HP:0011966"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000966", "HP:0000976", "HP:0000988", "HP:0001290", "HP:0001522", "HP:0001596", "HP:0001942", "HP:0003811", "HP:0011675", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000976", "HP:0000988", "HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0002013", "HP:0002027", "HP:0003819"], "RareDisease": ["OMIM:176000", "ORPHA:79276", "CCRD:92"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0001987", "HP:0002151", "HP:0002789", "HP:0003209", "HP:0003353", "HP:0003355", "HP:0008315", "HP:0010895", "HP:0040156"], "RareDisease": ["OMIM:253270", "ORPHA:79242", "CCRD:44"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003355", "HP:0003811", "HP:0010895", "HP:0010967", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001513", "HP:0003348", "HP:0010895", "HP:0010911", "HP:0010913", "HP:0010967", "HP:0011421"], "RareDisease": ["OMIM:243500", "ORPHA:33", "CCRD:58"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003573", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001270", "HP:0001272", "HP:0001522", "HP:0003075", "HP:0003146", "HP:0009125", "HP:0012642", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001257", "HP:0001522", "HP:0001945", "HP:0003150"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001051", "HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000639", "HP:0001251", "HP:0001315", "HP:0002151", "HP:0002490", "HP:0003150", "HP:0003542", "HP:0008315", "HP:0010701", "HP:0012117", "HP:0012318", "HP:0100613"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0012343"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0000961", "HP:0001290", "HP:0001522", "HP:0001662", "HP:0001943", "HP:0001987", "HP:0003215", "HP:0003811"], "RareDisease": ["OMIM:212138", "ORPHA:159"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001257", "HP:0001290", "HP:0001522", "HP:0001903", "HP:0001992", "HP:0002329", "HP:0002360"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000776", "HP:0001249", "HP:0001270", "HP:0001508", "HP:0001522", "HP:0002036", "HP:0002059", "HP:0009125", "HP:0011804"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001259", "HP:0001290", "HP:0001522", "HP:0001987", "HP:0002013", "HP:0002151", "HP:0002240", "HP:0002789", "HP:0003811", "HP:0011968", "HP:0012719", "HP:0200114"], "RareDisease": ["OMIM:207900", "ORPHA:23"], "Department": null}
{"Phenotype": ["HP:0000518", "HP:0001385", "HP:0001518", "HP:0001522", "HP:0001622", "HP:0001903", "HP:0001987", "HP:0003259", "HP:0003811", "HP:0003819", "HP:0010967", "HP:0012120", "HP:0100613"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000752", "HP:0001250", "HP:0001290", "HP:0001522", "HP:0002355", "HP:0003551", "HP:0003819", "HP:0009046", "HP:0040156"], "RareDisease": ["OMIM:271980", "ORPHA:22"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0040156", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000967", "HP:0001249", "HP:0001264", "HP:0001270", "HP:0001284", "HP:0001290", "HP:0001508", "HP:0001522", "HP:0002013", "HP:0002014", "HP:0002179", "HP:0002500", "HP:0002510", "HP:0002922", "HP:0003811", "HP:0003819", "HP:0008166", "HP:0011096", "HP:0011968", "HP:0100660"], "RareDisease": ["OMIM:245200", "ORPHA:487"], "Department": null}
{"Phenotype": ["HP:0000708", "HP:0000752", "HP:0001249", "HP:0001259", "HP:0001270", "HP:0001399", "HP:0001824", "HP:0001945", "HP:0001987", "HP:0002013", "HP:0002120", "HP:0002355", "HP:0003217", "HP:0003218", "HP:0003551", "HP:0003819", "HP:0009046", "HP:0010899", "HP:0010916", "HP:0011421"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001259", "HP:0001397", "HP:0001522", "HP:0002013", "HP:0002181", "HP:0012071"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000047", "HP:0001197", "HP:0001522", "HP:0002032", "HP:0002781", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0006510", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000742", "HP:0000750", "HP:0001249", "HP:0001250", "HP:0001522", "HP:0003231", "HP:0003510", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001290", "HP:0001522", "HP:0002093", "HP:0002151", "HP:0002329", "HP:0002360", "HP:0003215", "HP:0003688", "HP:0003811", "HP:0040156"], "RareDisease": ["OMIM:220110"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0011966"], "RareDisease": ["OMIM:605814", "ORPHA:247598", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000103", "HP:0000752", "HP:0001197", "HP:0001290", "HP:0001513", "HP:0001522", "HP:0001649", "HP:0001943", "HP:0002148", "HP:0002154", "HP:0002900", "HP:0002902", "HP:0002917", "HP:0003113", "HP:0003155", "HP:0003161", "HP:0003217", "HP:0003231", "HP:0003235", "HP:0003401", "HP:0003528", "HP:0003607", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0006254", "HP:0010551", "HP:0011421"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001249", "HP:0001270", "HP:0001522", "HP:0003231", "HP:0003819", "HP:0004923", "HP:0010472", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000750", "HP:0001249", "HP:0001250", "HP:0001513", "HP:0001520", "HP:0001522", "HP:0002060", "HP:0003811", "HP:0003819", "HP:0010908", "HP:0040144"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001270", "HP:0001290", "HP:0001513", "HP:0001522", "HP:0001987", "HP:0003811", "HP:0003819", "HP:0011421", "HP:0011966"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001249", "HP:0001270", "HP:0001522", "HP:0003231", "HP:0003510", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001051", "HP:0001522", "HP:0002151", "HP:0002286", "HP:0002299", "HP:0003348", "HP:0003811", "HP:0003819", "HP:0011364", "HP:0011421"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000316", "HP:0000369", "HP:0000431", "HP:0001197", "HP:0001249", "HP:0001270", "HP:0001522", "HP:0003781", "HP:0003811", "HP:0012071", "HP:0012714", "HP:0040081"], "RareDisease": ["OMIM:255120", "ORPHA:156"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001257", "HP:0001522", "HP:0001987", "HP:0002151", "HP:0002789", "HP:0003218", "HP:0003811", "HP:0045045"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0002305", "HP:0003150", "HP:0003530", "HP:0004429", "HP:0011968"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001987", "HP:0003218", "HP:0004322"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0010967"], "RareDisease": ["OMIM:201475", "ORPHA:26793", "CCRD:116"], "Department": null}
{"Phenotype": ["HP:0000752", "HP:0001254", "HP:0001259", "HP:0001298", "HP:0001317", "HP:0001332", "HP:0001649", "HP:0001919", "HP:0001945", "HP:0001974", "HP:0001987", "HP:0002060", "HP:0002071", "HP:0002153", "HP:0002329", "HP:0002360", "HP:0002910", "HP:0003228", "HP:0003819", "HP:0012378", "HP:0012622", "HP:0100660"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001522", "HP:0001945", "HP:0002014", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0004923", "HP:0010899", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000369", "HP:0000463", "HP:0000508", "HP:0000750", "HP:0000752", "HP:0001159", "HP:0001249", "HP:0001270", "HP:0001522", "HP:0002705", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0003819", "HP:0010442", "HP:0010569"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000750", "HP:0001197", "HP:0001249", "HP:0001251", "HP:0001270", "HP:0001522", "HP:0001987", "HP:0002179", "HP:0002240", "HP:0003355", "HP:0003811", "HP:0003819", "HP:0010907", "HP:0010909", "HP:0011966", "HP:0012127"], "RareDisease": ["OMIM:207900", "ORPHA:23"], "Department": null}
{"Phenotype": ["HP:0001513", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003231", "HP:0003819", "HP:0004429", "HP:0004923", "HP:0010472", "HP:0011421", "HP:0012343", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001257", "HP:0001522", "HP:0001987", "HP:0003645", "HP:0003811", "HP:0003819", "HP:0004342", "HP:0010899", "HP:0010916", "HP:0011968", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001622", "HP:0001987", "HP:0002240", "HP:0003573", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0008315", "HP:0010899", "HP:0010916", "HP:0040081", "HP:0100602"], "RareDisease": ["OMIM:212140", "ORPHA:158", "CCRD:15"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001622", "HP:0002155", "HP:0003811", "HP:0003819", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001259", "HP:0001265", "HP:0001290", "HP:0001522", "HP:0001649", "HP:0001942", "HP:0001987", "HP:0002098", "HP:0002181", "HP:0002380", "HP:0003573", "HP:0003645", "HP:0003811", "HP:0010899", "HP:0010903", "HP:0011965"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000752", "HP:0001249", "HP:0003819", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:271980", "ORPHA:22"], "Department": null}
{"Phenotype": ["HP:0000147", "HP:0000976", "HP:0000988", "HP:0001290", "HP:0001513", "HP:0001522", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0003231", "HP:0003819", "HP:0004386", "HP:0004429", "HP:0004923", "HP:0011421", "HP:0100613", "HP:0200039"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001513", "HP:0002027", "HP:0003819"], "RareDisease": ["OMIM:176000", "ORPHA:79276", "CCRD:92"], "Department": null}
{"Phenotype": ["HP:0001272", "HP:0001290", "HP:0001649", "HP:0001695", "HP:0003202", "HP:0003819", "HP:0004429", "HP:0009128", "HP:0012642", "HP:0040301"], "RareDisease": ["OMIM:307030", "ORPHA:408"], "Department": null}
{"Phenotype": ["HP:0001061", "HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001259", "HP:0001522", "HP:0001622", "HP:0001942", "HP:0001943", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0008315", "HP:0011421", "HP:0012418"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001987", "HP:0002154", "HP:0003348", "HP:0008315"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000742", "HP:0000750", "HP:0000961", "HP:0001000", "HP:0001197", "HP:0001250", "HP:0001522", "HP:0001944", "HP:0001945", "HP:0002153", "HP:0002900", "HP:0002902", "HP:0003811", "HP:0003819", "HP:0007832", "HP:0012714", "HP:0031213"], "RareDisease": ["OMIM:201910", "ORPHA:90794", "CCRD:1"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0003811", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000975", "HP:0001254", "HP:0001290", "HP:0001332", "HP:0001522", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0002094", "HP:0002329", "HP:0002360", "HP:0003150", "HP:0100660"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000238", "HP:0000348", "HP:0001257", "HP:0001290", "HP:0001522", "HP:0002059", "HP:0002305", "HP:0003150", "HP:0003819"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000752", "HP:0000998", "HP:0001249", "HP:0001257", "HP:0001259", "HP:0001290", "HP:0001513", "HP:0001522", "HP:0001987", "HP:0002090", "HP:0003218", "HP:0003532", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0010903", "HP:0010909", "HP:0010967", "HP:0011421", "HP:0011966", "HP:0011968", "HP:0012026", "HP:0012127", "HP:0100493", "HP:0100613", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0002013", "HP:0002076", "HP:0003217", "HP:0003218", "HP:0003348", "HP:0003572", "HP:0003819", "HP:0011421", "HP:0012127", "HP:0012343", "HP:0040126"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000476", "HP:0001522", "HP:0003150", "HP:0003530"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001264", "HP:0001522", "HP:0002120", "HP:0002179", "HP:0002305", "HP:0002510", "HP:0003150", "HP:0003530", "HP:0008315"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0001943", "HP:0002240", "HP:0002910", "HP:0003215", "HP:0003344", "HP:0004360", "HP:0008315", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0001250", "HP:0001522", "HP:0001903", "HP:0001945", "HP:0003150", "HP:0003819"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0003811", "HP:0040156"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0002910", "HP:0003155", "HP:0003573", "HP:0003645", "HP:0003811", "HP:0004342", "HP:0010899", "HP:0010916", "HP:0012024", "HP:0012343", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0010967", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000822", "HP:0000848", "HP:0001290", "HP:0001508", "HP:0001513", "HP:0001522", "HP:0002013", "HP:0002153", "HP:0002902", "HP:0003351", "HP:0003811", "HP:0003819", "HP:0008163", "HP:0011968", "HP:0031213"], "RareDisease": ["OMIM:201910", "ORPHA:90794", "CCRD:1"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0010899"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000047", "HP:0000252", "HP:0000307", "HP:0000331", "HP:0000463", "HP:0000473", "HP:0000486", "HP:0000540", "HP:0001159", "HP:0001249", "HP:0001265", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001622", "HP:0001662", "HP:0002104", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0010442", "HP:0010569", "HP:0011968"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0001942", "HP:0001987", "HP:0002013", "HP:0002154", "HP:0003217", "HP:0003218", "HP:0003348", "HP:0003355", "HP:0004353", "HP:0008315", "HP:0008358", "HP:0010909", "HP:0011421", "HP:0011966", "HP:0012127", "HP:0100613"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001508", "HP:0001522", "HP:0002240", "HP:0002910", "HP:0003161", "HP:0003231", "HP:0003235", "HP:0003355", "HP:0003607", "HP:0003645", "HP:0004923", "HP:0010916", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001249", "HP:0001513", "HP:0001522", "HP:0002060", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001272", "HP:0003819", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000750", "HP:0001249", "HP:0001250", "HP:0001522", "HP:0001945", "HP:0002060", "HP:0012714", "HP:0040144", "HP:0040147"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001250", "HP:0001290", "HP:0001522", "HP:0002179", "HP:0003811", "HP:0003819", "HP:0012321"], "RareDisease": ["OMIM:600721"], "Department": null}
{"Phenotype": ["HP:0000509", "HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000093", "HP:0000488", "HP:0000822", "HP:0001919", "HP:0012622", "HP:0040217", "HP:0100613"], "RareDisease": ["OMIM:125850", "ORPHA:552"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0003231", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001508", "HP:0001522", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001522", "HP:0001987", "HP:0002013", "HP:0002151", "HP:0002154", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0010967", "HP:0011421", "HP:0011968"], "RareDisease": ["OMIM:243500", "ORPHA:33", "CCRD:58"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000988", "HP:0001254", "HP:0001522", "HP:0001987", "HP:0002013", "HP:0002014", "HP:0002329", "HP:0002360", "HP:0003218", "HP:0008315", "HP:0025474", "HP:0025475", "HP:0030350"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001513", "HP:0001522", "HP:0001945", "HP:0002014", "HP:0002090", "HP:0002781", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0004923", "HP:0006510", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001251", "HP:0001270", "HP:0001290", "HP:0001513", "HP:0001522", "HP:0001733", "HP:0001873", "HP:0001877", "HP:0001882", "HP:0001942", "HP:0001944", "HP:0001987", "HP:0002013", "HP:0002014", "HP:0002090", "HP:0002149", "HP:0002151", "HP:0002154", "HP:0002751", "HP:0002912", "HP:0003075", "HP:0003138", "HP:0003259", "HP:0003348", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004429", "HP:0010472", "HP:0010967", "HP:0011421", "HP:0011968", "HP:0012120", "HP:0012714", "HP:0100806"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001284", "HP:0001290", "HP:0001522", "HP:0001987", "HP:0003811", "HP:0010899", "HP:0010916", "HP:0011968", "HP:0040156"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0012714", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0003468", "HP:0003819", "HP:0040319"], "RareDisease": ["OMIM:203500", "ORPHA:56"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000286", "HP:0000369", "HP:0000431", "HP:0000463", "HP:0000508", "HP:0001159", "HP:0001249", "HP:0001270", "HP:0001290", "HP:0001508", "HP:0001522", "HP:0002013", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0003819", "HP:0010442", "HP:0010569", "HP:0011968"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000741", "HP:0001290", "HP:0001522", "HP:0002013", "HP:0002014", "HP:0002059", "HP:0003150", "HP:0011968"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000509", "HP:0000750", "HP:0001510", "HP:0001513", "HP:0001518", "HP:0001522", "HP:0001622", "HP:0001877", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0010472", "HP:0012418"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001250", "HP:0001264", "HP:0001270", "HP:0001513", "HP:0001903", "HP:0001987", "HP:0002344", "HP:0002355", "HP:0002510", "HP:0003218", "HP:0003355", "HP:0003551", "HP:0003645", "HP:0003819", "HP:0009046", "HP:0010472", "HP:0010899", "HP:0010907", "HP:0010909", "HP:0010916", "HP:0011421", "HP:0012026", "HP:0012127", "HP:0025435", "HP:0100613", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:207800", "ORPHA:90", "CCRD:6"], "Department": null}
{"Phenotype": ["HP:0000478", "HP:0001166", "HP:0004950", "HP:0011421", "HP:0012638"], "RareDisease": ["OMIM:236200", "ORPHA:394", "CCRD:45"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001290", "HP:0001522", "HP:0001919", "HP:0001942", "HP:0001945", "HP:0001987", "HP:0002149", "HP:0002154", "HP:0002789", "HP:0002912", "HP:0003108", "HP:0003138", "HP:0003259", "HP:0003811", "HP:0010472", "HP:0010967", "HP:0011421", "HP:0012120", "HP:0012622", "HP:0040156"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0001249", "HP:0001250", "HP:0001254", "HP:0001257", "HP:0001290", "HP:0001522", "HP:0001987", "HP:0002329", "HP:0002360", "HP:0003811"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001259", "HP:0001397", "HP:0001522", "HP:0001943", "HP:0001987", "HP:0002013", "HP:0002239", "HP:0002900", "HP:0002910", "HP:0003215", "HP:0003344", "HP:0010472", "HP:0010895", "HP:0010899", "HP:0010916"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001250", "HP:0001254", "HP:0001522", "HP:0001942", "HP:0002013", "HP:0002329", "HP:0002360", "HP:0003811", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001629", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0002013", "HP:0003811", "HP:0010967", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001270", "HP:0001522", "HP:0003344", "HP:0003819", "HP:0040156"], "RareDisease": ["OMIM:250950", "ORPHA:67046"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000954", "HP:0000980", "HP:0001197", "HP:0001270", "HP:0001508", "HP:0001518", "HP:0001522", "HP:0001903", "HP:0001942", "HP:0001943", "HP:0001987", "HP:0002013", "HP:0002090", "HP:0002151", "HP:0002490", "HP:0003146", "HP:0003210", "HP:0003811", "HP:0010472", "HP:0010967", "HP:0011968", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0002120", "HP:0011421", "HP:0012120", "HP:0100613"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0010967", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001943", "HP:0003819", "HP:0008315", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:212140", "ORPHA:158", "CCRD:15"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001337", "HP:0002305", "HP:0011421", "HP:0040144", "HP:0100613"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000819", "HP:0012638", "HP:0040270", "HP:0100613"], "RareDisease": ["OMIM:125850", "ORPHA:552"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001251", "HP:0001513", "HP:0001522", "HP:0002104", "HP:0003231", "HP:0003401", "HP:0003811", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0002315", "HP:0003163", "HP:0003819"], "RareDisease": ["OMIM:176000", "ORPHA:79276", "CCRD:92"], "Department": null}
{"Phenotype": ["HP:0000670", "HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001250", "HP:0001290", "HP:0001522", "HP:0001622", "HP:0001943", "HP:0001974", "HP:0001987", "HP:0002155", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0010899", "HP:0010916", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001250", "HP:0001290", "HP:0001522", "HP:0001662", "HP:0002104", "HP:0002179", "HP:0003811", "HP:0004429", "HP:0010910", "HP:0010911", "HP:0010913", "HP:0012378", "HP:0500001"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0001649", "HP:0001945", "HP:0001987", "HP:0003110", "HP:0003811", "HP:0011968"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000976", "HP:0000988", "HP:0001522", "HP:0003131", "HP:0003268", "HP:0003297", "HP:0003532"], "RareDisease": ["OMIM:220100", "ORPHA:214"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001987", "HP:0003811", "HP:0003819", "HP:0011966"], "RareDisease": ["OMIM:605814", "ORPHA:247598", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001510", "HP:0001522", "HP:0001649", "HP:0001903", "HP:0002789", "HP:0003811", "HP:0012638", "HP:0040156"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001254", "HP:0001290", "HP:0001522", "HP:0002329", "HP:0002360", "HP:0003811", "HP:0011968", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003355", "HP:0003811", "HP:0010895", "HP:0010967", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000750", "HP:0001513", "HP:0001522", "HP:0001622", "HP:0003150", "HP:0003348", "HP:0003811", "HP:0003819", "HP:0010908", "HP:0010910", "HP:0010967", "HP:0011966", "HP:0012418"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000752", "HP:0001061", "HP:0001249", "HP:0001513", "HP:0003231", "HP:0003510", "HP:0003819", "HP:0004923", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001254", "HP:0001290", "HP:0002329", "HP:0002360", "HP:0002500", "HP:0003150", "HP:0003530", "HP:0003819", "HP:0011968"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0012318"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000726", "HP:0000988", "HP:0001257", "HP:0001284", "HP:0001522", "HP:0001945", "HP:0001987", "HP:0002014", "HP:0002181", "HP:0002240", "HP:0002344", "HP:0003297", "HP:0005961", "HP:0010901", "HP:0010903", "HP:0010916", "HP:0011966", "HP:0025474", "HP:0025475", "HP:0030350"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0001257", "HP:0002090", "HP:0003344", "HP:0003819", "HP:0004360"], "RareDisease": ["OMIM:250951", "ORPHA:67048"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001877", "HP:0001894", "HP:0003072", "HP:0003073", "HP:0003075", "HP:0003155", "HP:0003231", "HP:0003573", "HP:0004923", "HP:0006254", "HP:0010472", "HP:0012024"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0000545", "HP:0000662", "HP:0001987", "HP:0003819", "HP:0011421", "HP:0012026"], "RareDisease": ["OMIM:258870", "ORPHA:414"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001943", "HP:0002148", "HP:0002240", "HP:0002900", "HP:0003010", "HP:0003161", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0006254"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001290", "HP:0001510", "HP:0001522", "HP:0001629", "HP:0003468", "HP:0010280", "HP:0011356", "HP:0100758"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001250", "HP:0001264", "HP:0001270", "HP:0001332", "HP:0001522", "HP:0002305", "HP:0002510", "HP:0003150", "HP:0003510", "HP:0010551", "HP:0011421"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001250", "HP:0001251", "HP:0001522", "HP:0001945", "HP:0011421", "HP:0040144"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001942", "HP:0001987", "HP:0002789", "HP:0003209", "HP:0003353", "HP:0003355", "HP:0003811", "HP:0010895", "HP:0011968", "HP:0040156"], "RareDisease": ["OMIM:253270", "ORPHA:79242", "CCRD:44"], "Department": null}
{"Phenotype": ["HP:0000091", "HP:0000105", "HP:0000123", "HP:0000790", "HP:0000822", "HP:0001250", "HP:0001394", "HP:0001395", "HP:0001522", "HP:0001959", "HP:0002013", "HP:0002039", "HP:0002240", "HP:0003161", "HP:0003270", "HP:0003355", "HP:0003819", "HP:0006254", "HP:0010917", "HP:0031500"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0000488", "HP:0000518", "HP:0000822", "HP:0001635", "HP:0001658", "HP:0001919", "HP:0002344", "HP:0003076", "HP:0012622", "HP:0040217", "HP:0100613", "HP:0100806"], "RareDisease": ["OMIM:125850", "ORPHA:552"], "Department": null}
{"Phenotype": ["HP:0004923", "HP:0010917", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:276710"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001254", "HP:0001522", "HP:0001942", "HP:0001943", "HP:0002329", "HP:0002360", "HP:0003076", "HP:0003819", "HP:0011033"], "RareDisease": ["OMIM:229700", "ORPHA:348"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001522", "HP:0002013", "HP:0002312", "HP:0002370", "HP:0003811", "HP:0003819", "HP:0040301"], "RareDisease": ["OMIM:307030", "ORPHA:408"], "Department": null}
{"Phenotype": ["HP:0001272", "HP:0001298", "HP:0001522", "HP:0001999", "HP:0002683", "HP:0003811", "HP:0011421", "HP:0012642", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000518", "HP:0001197", "HP:0001399", "HP:0001522", "HP:0001631", "HP:0001987", "HP:0002908", "HP:0003573", "HP:0003607", "HP:0003645", "HP:0003811", "HP:0003819", "HP:0004342", "HP:0010899", "HP:0010916", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0010967", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0003819", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001251", "HP:0001522", "HP:0001654", "HP:0001987", "HP:0002154", "HP:0003510", "HP:0003819", "HP:0004429", "HP:0010472", "HP:0010967", "HP:0011421", "HP:0012714", "HP:0100613"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000741", "HP:0000750", "HP:0001250", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001596", "HP:0003270", "HP:0003353", "HP:0003819", "HP:0004429", "HP:0010899", "HP:0010916", "HP:0012714", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000486", "HP:0000750", "HP:0001250", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001622", "HP:0001987", "HP:0003811", "HP:0004386", "HP:0004429", "HP:0010903", "HP:0011968"], "RareDisease": ["OMIM:237310", "ORPHA:927", "CCRD:79"], "Department": null}
{"Phenotype": ["HP:0001919", "HP:0002912", "HP:0008315", "HP:0010472", "HP:0011421", "HP:0012100", "HP:0012120", "HP:0012622", "HP:0100613"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000486", "HP:0000741", "HP:0000752", "HP:0001249", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0001987", "HP:0002013", "HP:0002154", "HP:0003348", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0010911", "HP:0010967", "HP:0011421", "HP:0011968"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001270", "HP:0001290", "HP:0001518", "HP:0001522", "HP:0001622", "HP:0001945", "HP:0001987", "HP:0002013", "HP:0002151", "HP:0003155", "HP:0003218", "HP:0003355", "HP:0003811", "HP:0003819", "HP:0010895", "HP:0010899", "HP:0010907", "HP:0010909", "HP:0010911", "HP:0010916", "HP:0010967", "HP:0011966", "HP:0011968", "HP:0012378"], "RareDisease": ["OMIM:207900", "ORPHA:23"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000737", "HP:0000975", "HP:0001254", "HP:0001290", "HP:0001332", "HP:0001522", "HP:0001944", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0002329", "HP:0002360", "HP:0003150", "HP:0003530", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0011968", "HP:0100660"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001695", "HP:0003150"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000421", "HP:0000670", "HP:0001522", "HP:0001649", "HP:0003811", "HP:0003819", "HP:0004342"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001051", "HP:0001250", "HP:0001265", "HP:0001290", "HP:0001522", "HP:0003355", "HP:0010895", "HP:0040156", "HP:0500001"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0001250", "HP:0001254", "HP:0001270", "HP:0001508", "HP:0001522", "HP:0001824", "HP:0001987", "HP:0002181", "HP:0002329", "HP:0002360", "HP:0003218", "HP:0003268", "HP:0004429", "HP:0010909", "HP:0011968", "HP:0012127"], "RareDisease": ["OMIM:207800", "ORPHA:90", "CCRD:6"], "Department": null}
{"Phenotype": ["HP:0000518", "HP:0000750", "HP:0001081", "HP:0001249", "HP:0001257", "HP:0001508", "HP:0001522", "HP:0001760", "HP:0002013", "HP:0002240", "HP:0002910", "HP:0003155", "HP:0003811", "HP:0003819", "HP:0004342", "HP:0010899", "HP:0010916", "HP:0011421", "HP:0011968", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001987", "HP:0002094", "HP:0003110", "HP:0003811", "HP:0012638"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001397", "HP:0002910", "HP:0003819", "HP:0004923", "HP:0010837", "HP:0010839", "HP:0010899", "HP:0010916", "HP:0011967"], "RareDisease": ["OMIM:277900", "ORPHA:905", "CCRD:37"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0001251", "HP:0001259", "HP:0001522", "HP:0001987", "HP:0002013", "HP:0002014", "HP:0002151", "HP:0002401", "HP:0004429", "HP:0010910", "HP:0010911", "HP:0010913", "HP:0011421"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001332", "HP:0001760", "HP:0002355", "HP:0003202", "HP:0003231", "HP:0003551", "HP:0003819", "HP:0004923", "HP:0005781", "HP:0009046", "HP:0009128", "HP:0010472", "HP:0011421"], "RareDisease": ["OMIM:128230", "ORPHA:98808"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001513", "HP:0001522", "HP:0001629", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000158", "HP:0000256", "HP:0000280", "HP:0000752", "HP:0001744", "HP:0002240", "HP:0003819", "HP:0004429", "HP:0011421", "HP:0011968"], "RareDisease": ["OMIM:309900", "ORPHA:580", "CCRD:73"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000822", "HP:0000939", "HP:0001254", "HP:0001264", "HP:0001290", "HP:0001347", "HP:0001649", "HP:0001760", "HP:0001903", "HP:0001919", "HP:0001945", "HP:0001987", "HP:0002013", "HP:0002149", "HP:0002153", "HP:0002154", "HP:0002209", "HP:0002329", "HP:0002355", "HP:0002360", "HP:0002510", "HP:0003072", "HP:0003075", "HP:0003138", "HP:0003210", "HP:0003228", "HP:0003259", "HP:0003348", "HP:0003510", "HP:0003551", "HP:0003819", "HP:0004357", "HP:0004429", "HP:0009046", "HP:0010472", "HP:0010912", "HP:0010914", "HP:0010967", "HP:0011421", "HP:0012120", "HP:0012239", "HP:0012622", "HP:0012714", "HP:0040081", "HP:0100613"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001270", "HP:0001290", "HP:0002013", "HP:0003217", "HP:0003819", "HP:0004429", "HP:0010911", "HP:0011968", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000509", "HP:0001522", "HP:0003811", "HP:0011966"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000962", "HP:0000976", "HP:0000988", "HP:0001197", "HP:0001522", "HP:0001642", "HP:0002239", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001290", "HP:0001522", "HP:0001987", "HP:0002329", "HP:0002360", "HP:0003811", "HP:0010910", "HP:0010911", "HP:0010918", "HP:0100806", "HP:0200114"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001513", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001272", "HP:0001508", "HP:0001522", "HP:0002910", "HP:0011968", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000158", "HP:0000431", "HP:0001249", "HP:0001251", "HP:0001270", "HP:0001284", "HP:0001290", "HP:0001522", "HP:0001760", "HP:0002090", "HP:0002355", "HP:0002751", "HP:0003202", "HP:0003270", "HP:0003551", "HP:0003819", "HP:0008064", "HP:0009046", "HP:0009128", "HP:0010571", "HP:0011421", "HP:0012714"], "RareDisease": ["OMIM:266500", "ORPHA:773"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000252", "HP:0000286", "HP:0000369", "HP:0000463", "HP:0000486", "HP:0000508", "HP:0000639", "HP:0000750", "HP:0001052", "HP:0001159", "HP:0001249", "HP:0001254", "HP:0001270", "HP:0001290", "HP:0001508", "HP:0001522", "HP:0002305", "HP:0002329", "HP:0002360", "HP:0003124", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0003819", "HP:0010569", "HP:0011968"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001264", "HP:0001298", "HP:0001522", "HP:0001945", "HP:0002510", "HP:0002789", "HP:0003150"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0001629", "HP:0001631", "HP:0001903", "HP:0001943", "HP:0002240", "HP:0002789", "HP:0003215", "HP:0003535", "HP:0003811", "HP:0011968", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001944", "HP:0001945", "HP:0002013", "HP:0002098", "HP:0002912", "HP:0003108", "HP:0003124", "HP:0003348", "HP:0003819", "HP:0010472", "HP:0010967", "HP:0012120"], "RareDisease": ["OMIM:251100", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0001596", "HP:0003819", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0002020", "HP:0002151", "HP:0002248", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001942", "HP:0001945", "HP:0001987", "HP:0002013", "HP:0002240", "HP:0002789", "HP:0003215", "HP:0003344", "HP:0003811", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001290", "HP:0001332", "HP:0001522", "HP:0001942", "HP:0003150", "HP:0008315", "HP:0100660"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003811", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0003131", "HP:0003268", "HP:0003532", "HP:0010908", "HP:0011421"], "RareDisease": ["OMIM:220100", "ORPHA:214"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001272", "HP:0001522", "HP:0002240", "HP:0003075", "HP:0003146", "HP:0009125", "HP:0012642", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000939", "HP:0001290", "HP:0001513", "HP:0001760", "HP:0001882", "HP:0001987", "HP:0002154", "HP:0002312", "HP:0002370", "HP:0003348", "HP:0003510", "HP:0003819", "HP:0004386", "HP:0010472", "HP:0010899", "HP:0010911", "HP:0010967", "HP:0011421", "HP:0012714", "HP:0100613"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0000980", "HP:0001522", "HP:0001541", "HP:0001894", "HP:0001903", "HP:0002240", "HP:0003073", "HP:0003075", "HP:0003155", "HP:0003231", "HP:0003355", "HP:0006254", "HP:0010472", "HP:0200039"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001249", "HP:0001270", "HP:0001272", "HP:0001337", "HP:0003819", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0002013", "HP:0003215", "HP:0003355", "HP:0003811", "HP:0004357", "HP:0010912", "HP:0040156"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000289", "HP:0000343", "HP:0000431", "HP:0000463", "HP:0000501", "HP:0000518", "HP:0000811", "HP:0001159", "HP:0001290", "HP:0001522", "HP:0002002", "HP:0002013", "HP:0002021", "HP:0002705", "HP:0003146", "HP:0003270", "HP:0003462", "HP:0003811", "HP:0010569", "HP:0011968"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001259", "HP:0001270", "HP:0001290", "HP:0001332", "HP:0001522", "HP:0001942", "HP:0001943", "HP:0001987", "HP:0002098", "HP:0003819", "HP:0010895", "HP:0011968", "HP:0040156"], "RareDisease": ["OMIM:203750", "ORPHA:134", "CCRD:12"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001332", "HP:0001522", "HP:0003150", "HP:0010551", "HP:0011968"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000324", "HP:0000473", "HP:0000608", "HP:0000750", "HP:0000752", "HP:0001250", "HP:0001251", "HP:0001264", "HP:0001522", "HP:0002014", "HP:0002059", "HP:0002090", "HP:0002179", "HP:0002305", "HP:0002510", "HP:0002538", "HP:0003811", "HP:0003819", "HP:0100660"], "RareDisease": ["OMIM:256730"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0001662", "HP:0002045", "HP:0002104", "HP:0003571", "HP:0003811", "HP:0011968", "HP:0012378"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0002151", "HP:0003811"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000976", "HP:0000988", "HP:0001250", "HP:0001254", "HP:0001522", "HP:0002019", "HP:0002093", "HP:0002329", "HP:0002360", "HP:0003219", "HP:0003688", "HP:0010895"], "RareDisease": ["OMIM:220110"], "Department": null}
{"Phenotype": ["HP:0000961", "HP:0001250", "HP:0001522", "HP:0001662", "HP:0001919", "HP:0002013", "HP:0002093", "HP:0002151", "HP:0002153", "HP:0002248", "HP:0003215", "HP:0003535", "HP:0003781", "HP:0003811", "HP:0010899", "HP:0012418", "HP:0012622", "HP:0025435", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000010", "HP:0000123", "HP:0000790", "HP:0001522", "HP:0003131", "HP:0003268", "HP:0003297", "HP:0003532"], "RareDisease": ["OMIM:220100", "ORPHA:214"], "Department": null}
{"Phenotype": ["HP:0003355", "HP:0010895", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0001254", "HP:0001290", "HP:0001332", "HP:0001522", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0002094", "HP:0002305", "HP:0002329", "HP:0002360", "HP:0003150", "HP:0003530", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0100660"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001522", "HP:0001873", "HP:0001882", "HP:0001943", "HP:0001944", "HP:0001945", "HP:0001987", "HP:0002027", "HP:0002045", "HP:0002090", "HP:0002154", "HP:0002329", "HP:0002360", "HP:0003348", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0005561", "HP:0010910", "HP:0010913", "HP:0010967", "HP:0011421", "HP:0011968", "HP:0012378", "HP:0500001"], "RareDisease": ["OMIM:243500", "ORPHA:33", "CCRD:58"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000648", "HP:0000750", "HP:0001249", "HP:0001250", "HP:0001251", "HP:0001264", "HP:0001907", "HP:0002160", "HP:0002510", "HP:0003658", "HP:0003819", "HP:0011421"], "RareDisease": ["OMIM:236250"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0002013", "HP:0002014", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001943", "HP:0003355", "HP:0003811", "HP:0010895", "HP:0010967", "HP:0012638", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000750", "HP:0001249", "HP:0001394", "HP:0001395", "HP:0001522", "HP:0002149", "HP:0002896", "HP:0003155", "HP:0003161", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0006254", "HP:0010472", "HP:0010899", "HP:0010916", "HP:0011421", "HP:0012343", "HP:0040303"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001522", "HP:0001942", "HP:0001987", "HP:0002013", "HP:0002045", "HP:0002090", "HP:0002154", "HP:0002240", "HP:0002329", "HP:0002360", "HP:0002910", "HP:0003108", "HP:0003155", "HP:0003215", "HP:0003217", "HP:0003218", "HP:0003348", "HP:0003645", "HP:0003819", "HP:0004353", "HP:0004429", "HP:0010899", "HP:0010907", "HP:0011421", "HP:0011966", "HP:0012127", "HP:0012378", "HP:0025435", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001943", "HP:0001944", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0008315", "HP:0012378"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000976", "HP:0000988", "HP:0001197", "HP:0001522", "HP:0001945", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001270", "HP:0001513", "HP:0001522", "HP:0001622", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0004923", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001510", "HP:0001522", "HP:0002013", "HP:0003811", "HP:0011968", "HP:0040156", "HP:0500001"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0000047", "HP:0000252", "HP:0001197", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0003161", "HP:0003231", "HP:0003607", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0006254"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0001265", "HP:0001290", "HP:0001397", "HP:0001522", "HP:0001649", "HP:0001944", "HP:0001945", "HP:0002013", "HP:0002027", "HP:0002094", "HP:0002151", "HP:0002155", "HP:0002240", "HP:0002789", "HP:0003202", "HP:0003348", "HP:0003355", "HP:0003811", "HP:0009128", "HP:0011968", "HP:0012447", "HP:0031500"], "RareDisease": ["OMIM:229600", "ORPHA:469", "CCRD:40"], "Department": null}
{"Phenotype": ["HP:0001270", "HP:0001290", "HP:0001522", "HP:0002305", "HP:0003150", "HP:0045045", "HP:0100660"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001622", "HP:0001987", "HP:0002090", "HP:0002686", "HP:0003811", "HP:0003819", "HP:0005961", "HP:0011966", "HP:0100790"], "RareDisease": ["OMIM:605814", "ORPHA:247598", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001907", "HP:0002160", "HP:0003235", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:236200", "ORPHA:394", "CCRD:45"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001513", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011421", "HP:0040156", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001290", "HP:0001522", "HP:0001943", "HP:0001987", "HP:0002013", "HP:0002329", "HP:0002360", "HP:0003819", "HP:0008315"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003150", "HP:0003811"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000047", "HP:0000750", "HP:0001197", "HP:0001290", "HP:0001522", "HP:0002355", "HP:0003551", "HP:0003811", "HP:0003819", "HP:0009046"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0002329", "HP:0002360", "HP:0002653", "HP:0003231", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001254", "HP:0001290", "HP:0001513", "HP:0001522", "HP:0001987", "HP:0002013", "HP:0002329", "HP:0002360", "HP:0003217", "HP:0003218", "HP:0003348", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0010899", "HP:0010909", "HP:0011421", "HP:0011966", "HP:0011968"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0003819", "HP:0011421", "HP:0040270", "HP:0100613"], "RareDisease": ["OMIM:125850", "ORPHA:552"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0001942", "HP:0003150", "HP:0003811", "HP:0008315"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0003215", "HP:0003344", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003231", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000709", "HP:0000976", "HP:0000988", "HP:0001249", "HP:0001522", "HP:0002027", "HP:0002321", "HP:0003231", "HP:0004923", "HP:0012318", "HP:0040156", "HP:0100613", "HP:0200039"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001877", "HP:0001894", "HP:0003811", "HP:0003819", "HP:0004342", "HP:0010472", "HP:0100511"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0002013", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004429", "HP:0008315", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0001649", "HP:0001942", "HP:0001945", "HP:0001987", "HP:0002151", "HP:0002380", "HP:0002789", "HP:0003811", "HP:0011965", "HP:0011968"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001987", "HP:0003811", "HP:0003819", "HP:0011966", "HP:0012127"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000670", "HP:0000750", "HP:0001249", "HP:0001250", "HP:0001264", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001987", "HP:0002013", "HP:0002014", "HP:0002093", "HP:0002355", "HP:0002510", "HP:0003551", "HP:0003781", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0009046", "HP:0010910", "HP:0010911", "HP:0010913", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001518", "HP:0001522", "HP:0001987", "HP:0003355", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0010895", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0003401", "HP:0004923", "HP:0100613", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0003819", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001249", "HP:0001522", "HP:0003296", "HP:0003811", "HP:0003819", "HP:0004342", "HP:0010899", "HP:0010916", "HP:0010917", "HP:0012023", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001903", "HP:0002160", "HP:0010472", "HP:0040087", "HP:0040126"], "RareDisease": ["OMIM:236200", "ORPHA:394", "CCRD:45"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000123", "HP:0001508", "HP:0001522", "HP:0002013", "HP:0002014", "HP:0002240", "HP:0010917", "HP:0040156"], "RareDisease": ["OMIM:140350", "ORPHA:2118"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001522", "HP:0003218", "HP:0003811", "HP:0011968", "HP:0100806"], "RareDisease": ["OMIM:207900", "ORPHA:23"], "Department": null}
{"Phenotype": ["HP:0000952", "HP:0001197", "HP:0001522", "HP:0002908", "HP:0003155", "HP:0003231", "HP:0003573", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000967", "HP:0001000", "HP:0001522", "HP:0001873", "HP:0001943", "HP:0001987", "HP:0003155", "HP:0003161", "HP:0003231", "HP:0003235", "HP:0003645", "HP:0003819", "HP:0004923", "HP:0006254", "HP:0007832", "HP:0008064", "HP:0010472"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000047", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001290", "HP:0001298", "HP:0001508", "HP:0001513", "HP:0001522", "HP:0001882", "HP:0001974", "HP:0001987", "HP:0002021", "HP:0002093", "HP:0002154", "HP:0003811", "HP:0003819", "HP:0010899", "HP:0010916", "HP:0010967", "HP:0011421", "HP:0011968", "HP:0100806"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0008315"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000570", "HP:0000649", "HP:0001250", "HP:0001257", "HP:0001522", "HP:0001943", "HP:0001945", "HP:0001987", "HP:0002060", "HP:0003150", "HP:0003530", "HP:0008315", "HP:0010551", "HP:0045045"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001522", "HP:0003110", "HP:0003811", "HP:0003819"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001251", "HP:0001260", "HP:0001264", "HP:0001270", "HP:0001290", "HP:0001347", "HP:0001510", "HP:0001522", "HP:0001760", "HP:0002014", "HP:0002134", "HP:0002151", "HP:0002510", "HP:0003219", "HP:0003542", "HP:0003688", "HP:0003819", "HP:0011421"], "RareDisease": ["OMIM:220110"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0001945", "HP:0002060", "HP:0003150", "HP:0008315", "HP:0011220", "HP:0011968"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001249", "HP:0001251", "HP:0001270", "HP:0001272", "HP:0001290", "HP:0003819", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001522", "HP:0001942", "HP:0002789", "HP:0003344", "HP:0003811"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0000976", "HP:0000988", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0001987", "HP:0002013", "HP:0002151", "HP:0002240", "HP:0003209", "HP:0003353", "HP:0003355", "HP:0010895", "HP:0011968", "HP:0040156"], "RareDisease": ["OMIM:253270", "ORPHA:79242", "CCRD:44"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0001824", "HP:0001945", "HP:0002094", "HP:0003218", "HP:0003811", "HP:0030215"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001298", "HP:0001522", "HP:0001943", "HP:0001987", "HP:0002151", "HP:0002500", "HP:0003150", "HP:0003344", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004429", "HP:0010967", "HP:0010996", "HP:0011968", "HP:0040156"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0003510", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0000842", "HP:0001197", "HP:0001522", "HP:0001873", "HP:0001892", "HP:0001943", "HP:0001987", "HP:0003155", "HP:0003161", "HP:0003231", "HP:0003235", "HP:0003645", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0006254", "HP:0010472", "HP:0012117"], "RareDisease": ["OMIM:276700", "ORPHA:882", "CCRD:115.1"], "Department": null}
{"Phenotype": ["HP:0000121", "HP:0000421", "HP:0001508", "HP:0001522", "HP:0001642", "HP:0002151", "HP:0002240", "HP:0002900", "HP:0002918", "HP:0003124", "HP:0031415", "HP:0003155", "HP:0003348", "HP:0003355", "HP:0003452", "HP:0003510", "HP:0003537", "HP:0003819", "HP:0010472", "HP:0010899", "HP:0011421"], "RareDisease": ["OMIM:227810"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0003215", "HP:0003811", "HP:0011968"], "RareDisease": ["OMIM:232200", "CCRD:35.1"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001254", "HP:0001522", "HP:0001649", "HP:0001942", "HP:0001943", "HP:0002013", "HP:0002151", "HP:0002329", "HP:0002360", "HP:0002789", "HP:0011968", "HP:0040155"], "RareDisease": ["OMIM:229700", "ORPHA:348"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001249", "HP:0001257", "HP:0001270", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0001249", "HP:0001270", "HP:0001522", "HP:0001942", "HP:0001987", "HP:0002154", "HP:0002179", "HP:0002912", "HP:0003210", "HP:0003811", "HP:0010910", "HP:0010967", "HP:0011968", "HP:0012100", "HP:0012120", "HP:0100511", "HP:0100613"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000670", "HP:0000750", "HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000123", "HP:0001508", "HP:0001510", "HP:0001522", "HP:0002013", "HP:0002014", "HP:0010917", "HP:0040156"], "RareDisease": ["OMIM:140350", "ORPHA:2118"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000486", "HP:0000639", "HP:0000648", "HP:0000742", "HP:0001141", "HP:0001249", "HP:0001250", "HP:0001254", "HP:0001270", "HP:0001396", "HP:0001508", "HP:0001522", "HP:0001629", "HP:0001873", "HP:0001875", "HP:0001882", "HP:0001903", "HP:0001987", "HP:0002098", "HP:0002160", "HP:0002240", "HP:0002329", "HP:0002360", "HP:0002813", "HP:0003235", "HP:0003658", "HP:0003811", "HP:0003819", "HP:0004360", "HP:0008315", "HP:0010995", "HP:0012120", "HP:0100660"], "RareDisease": ["OMIM:277400", "ORPHA:79282", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004429", "HP:0010910", "HP:0010911", "HP:0010913", "HP:0011421", "HP:0100613", "HP:0200039"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001290", "HP:0001397", "HP:0001522", "HP:0001640", "HP:0001698", "HP:0001942", "HP:0001943", "HP:0001987", "HP:0002013", "HP:0002014", "HP:0002094", "HP:0002240", "HP:0002329", "HP:0002360", "HP:0002789", "HP:0006688", "HP:0008315", "HP:0010899", "HP:0010916", "HP:0025435"], "RareDisease": ["OMIM:201475", "ORPHA:26793", "CCRD:116"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0003510", "HP:0003819", "HP:0004342"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0002355", "HP:0003326", "HP:0003551", "HP:0003752", "HP:0003819", "HP:0009046", "HP:0010899", "HP:0010967", "HP:0040081", "HP:0200072"], "RareDisease": ["OMIM:255110", "ORPHA:228302"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000486", "HP:0000750", "HP:0001250", "HP:0001251", "HP:0001254", "HP:0001522", "HP:0002060", "HP:0002151", "HP:0002329", "HP:0002344", "HP:0002360", "HP:0003819", "HP:0010899"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0000010", "HP:0001522", "HP:0003131", "HP:0003268", "HP:0003297", "HP:0003532"], "RareDisease": ["OMIM:220100", "ORPHA:214"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001945", "HP:0003231", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000819", "HP:0001249", "HP:0001250", "HP:0001522", "HP:0002500", "HP:0003231", "HP:0004923", "HP:0100613", "HP:0500001"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000790", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0002014", "HP:0002151", "HP:0002490", "HP:0011968", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001249", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0001249", "HP:0001513", "HP:0001522", "HP:0001744", "HP:0001987", "HP:0002013", "HP:0002161", "HP:0002240", "HP:0002910", "HP:0003155", "HP:0003217", "HP:0003218", "HP:0003348", "HP:0003530", "HP:0003572", "HP:0003645", "HP:0004429", "HP:0010909", "HP:0011421", "HP:0012025", "HP:0012127", "HP:0040081"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000980", "HP:0001249", "HP:0001254", "HP:0001290", "HP:0001522", "HP:0001882", "HP:0001903", "HP:0001987", "HP:0002154", "HP:0002329", "HP:0002360", "HP:0003348", "HP:0003819", "HP:0010472", "HP:0010967", "HP:0012239", "HP:0012714", "HP:0040156"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001249", "HP:0001251", "HP:0001270", "HP:0001272", "HP:0001513", "HP:0001522", "HP:0001907", "HP:0003819", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001510", "HP:0001522", "HP:0010628", "HP:0040319"], "RareDisease": ["OMIM:203500", "ORPHA:56"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0000961", "HP:0001250", "HP:0001522", "HP:0001987", "HP:0002179", "HP:0002181", "HP:0003218", "HP:0003811", "HP:0011968"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0000750", "HP:0001250", "HP:0001270", "HP:0001290", "HP:0001399", "HP:0001510", "HP:0001522", "HP:0001635", "HP:0001733", "HP:0001738", "HP:0001873", "HP:0001882", "HP:0001903", "HP:0001919", "HP:0001944", "HP:0001987", "HP:0002090", "HP:0002149", "HP:0002151", "HP:0002154", "HP:0002181", "HP:0002209", "HP:0002240", "HP:0002910", "HP:0003108", "HP:0003138", "HP:0003259", "HP:0003348", "HP:0003645", "HP:0003819", "HP:0004429", "HP:0010899", "HP:0010903", "HP:0010912", "HP:0010914", "HP:0010918", "HP:0010967", "HP:0010996", "HP:0012622", "HP:0025435", "HP:0040156"], "RareDisease": ["OMIM:606054", "ORPHA:35", "CCRD:99"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001254", "HP:0001347", "HP:0001945", "HP:0001987", "HP:0002013", "HP:0002181", "HP:0002329", "HP:0002360", "HP:0003218", "HP:0003819", "HP:0012025"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0000961", "HP:0001250", "HP:0001522", "HP:0001662", "HP:0002013", "HP:0003215", "HP:0003811"], "RareDisease": ["OMIM:246450", "ORPHA:20"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0004923", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000752", "HP:0001249", "HP:0001250", "HP:0001290", "HP:0003819", "HP:0008315", "HP:0010996", "HP:0040156"], "RareDisease": ["OMIM:271980", "ORPHA:22"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0008315", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003231", "HP:0003819", "HP:0004923", "HP:0200039"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000486", "HP:0000821", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001522", "HP:0002019", "HP:0002925", "HP:0003231", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0001760", "HP:0001945", "HP:0002789", "HP:0003811", "HP:0003819", "HP:0008315"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923", "HP:0040156", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001638", "HP:0008315", "HP:0011421", "HP:0012071"], "RareDisease": ["OMIM:212140", "ORPHA:158", "CCRD:15"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001513", "HP:0003231", "HP:0004923", "HP:0040126", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001259", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0001945", "HP:0001987", "HP:0002013", "HP:0002014", "HP:0002045", "HP:0002094", "HP:0002179", "HP:0002181", "HP:0002789", "HP:0003076", "HP:0003645", "HP:0003811", "HP:0004429", "HP:0100806"], "RareDisease": ["OMIM:237300", "ORPHA:147"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001508", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000618", "HP:0001270", "HP:0001347", "HP:0001522", "HP:0002179", "HP:0010899"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0000670", "HP:0001249", "HP:0003819", "HP:0004923", "HP:0008064", "HP:0010917", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000047", "HP:0000054", "HP:0000509", "HP:0001520", "HP:0001522", "HP:0001944", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0002153", "HP:0002902", "HP:0003072", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0011968", "HP:0012318", "HP:0030088", "HP:0031213"], "RareDisease": ["OMIM:201810", "ORPHA:90791"], "Department": null}
{"Phenotype": ["HP:0000975", "HP:0000988", "HP:0001197", "HP:0001290", "HP:0001522", "HP:0003155", "HP:0003219", "HP:0003231", "HP:0003348", "HP:0003811", "HP:0010899", "HP:0010967", "HP:0025474", "HP:0025475", "HP:0030350", "HP:0040081"], "RareDisease": ["OMIM:201470"], "Department": null}
{"Phenotype": ["HP:0000100", "HP:0001337", "HP:0003819", "HP:0040144"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0001824", "HP:0001987", "HP:0002013", "HP:0002151", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000750", "HP:0003819", "HP:0040144"], "RareDisease": ["OMIM:236792", "ORPHA:79314"], "Department": null}
{"Phenotype": ["HP:0000670", "HP:0001249", "HP:0001281", "HP:0001290", "HP:0001508", "HP:0001522", "HP:0002240", "HP:0002653", "HP:0002900", "HP:0003124", "HP:0031415", "HP:0003155", "HP:0003510", "HP:0003819", "HP:0008315", "HP:0011421"], "RareDisease": ["OMIM:227810"], "Department": null}
{"Phenotype": ["HP:0000238", "HP:0001522", "HP:0001903", "HP:0003150", "HP:0003530", "HP:0008315"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000570", "HP:0001272", "HP:0001290", "HP:0001522", "HP:0001907", "HP:0003811", "HP:0009125", "HP:0011842", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0000509", "HP:0000613", "HP:0000962", "HP:0001249", "HP:0001250", "HP:0003231", "HP:0003819", "HP:0009926"], "RareDisease": ["OMIM:276600", "ORPHA:28378"], "Department": null}
{"Phenotype": ["HP:0000967", "HP:0001250", "HP:0001254", "HP:0001290", "HP:0001315", "HP:0001522", "HP:0002151", "HP:0002329", "HP:0002360", "HP:0003150", "HP:0003202", "HP:0003219", "HP:0003688", "HP:0009128"], "RareDisease": ["OMIM:220110"], "Department": null}
{"Phenotype": ["HP:0000369", "HP:0000639", "HP:0001257", "HP:0001522", "HP:0002094", "HP:0002286", "HP:0002705", "HP:0003573", "HP:0003811", "HP:0010307", "HP:0011364", "HP:0011968", "HP:0012378"], "RareDisease": ["OMIM:266130"], "Department": null}
{"Phenotype": ["HP:0003131", "HP:0003268", "HP:0010909", "HP:0011965", "HP:0012127"], "RareDisease": ["OMIM:207800", "ORPHA:90", "CCRD:6"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003811", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001272", "HP:0003819", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001522", "HP:0001987", "HP:0002013", "HP:0002329", "HP:0002360", "HP:0003217", "HP:0003218", "HP:0012025"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000737", "HP:0001265", "HP:0001522", "HP:0001987", "HP:0002179", "HP:0002305", "HP:0010899"], "RareDisease": ["OMIM:271900", "ORPHA:141"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001315", "HP:0001522", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0003150"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000752", "HP:0001249", "HP:0001513", "HP:0001522", "HP:0001987", "HP:0003811", "HP:0003819", "HP:0008064", "HP:0011421", "HP:0011966"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001259", "HP:0001945", "HP:0002013", "HP:0002789", "HP:0003819", "HP:0010910", "HP:0010913", "HP:0011968"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0000238", "HP:0001250", "HP:0001251", "HP:0001290", "HP:0001522", "HP:0003355", "HP:0003811", "HP:0010895", "HP:0040156"], "RareDisease": ["OMIM:210200", "ORPHA:6"], "Department": null}
{"Phenotype": ["HP:0001264", "HP:0001522", "HP:0002510", "HP:0040319"], "RareDisease": ["OMIM:203500", "ORPHA:56"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000750", "HP:0001249", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001877", "HP:0001882", "HP:0001942", "HP:0001943", "HP:0001987", "HP:0002134", "HP:0002149", "HP:0002154", "HP:0002240", "HP:0002355", "HP:0002912", "HP:0003075", "HP:0003138", "HP:0003510", "HP:0003551", "HP:0003811", "HP:0003819", "HP:0007109", "HP:0009046", "HP:0010472", "HP:0010967", "HP:0011421", "HP:0012120", "HP:0012447"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001622", "HP:0001987", "HP:0003811", "HP:0011966"], "RareDisease": ["OMIM:215700", "ORPHA:247525", "CCRD:18"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000545", "HP:0000750", "HP:0001083", "HP:0001270", "HP:0001298", "HP:0001373", "HP:0001382", "HP:0002160", "HP:0002181", "HP:0002312", "HP:0002370", "HP:0003235", "HP:0003355", "HP:0003819", "HP:0011421"], "RareDisease": ["OMIM:236200", "ORPHA:394", "CCRD:45"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001249", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011421"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001522", "HP:0001824", "HP:0001944", "HP:0001987", "HP:0002090", "HP:0002094", "HP:0002179", "HP:0002181", "HP:0002329", "HP:0002360", "HP:0002789", "HP:0003217", "HP:0003218", "HP:0003348", "HP:0003355", "HP:0003811", "HP:0003819", "HP:0004353", "HP:0004386", "HP:0004429", "HP:0010899", "HP:0010907", "HP:0010909", "HP:0010967", "HP:0011421", "HP:0011966", "HP:0012127", "HP:0040156"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0001250", "HP:0001522", "HP:0002179", "HP:0003150", "HP:0003530", "HP:0003811"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0003819", "HP:0004429", "HP:0010967", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000741", "HP:0000961", "HP:0001251", "HP:0001347", "HP:0001522", "HP:0001942", "HP:0001943", "HP:0002013", "HP:0002045", "HP:0002154", "HP:0002912", "HP:0003210", "HP:0003348", "HP:0003819", "HP:0004429", "HP:0010909", "HP:0010910", "HP:0010967", "HP:0011966", "HP:0012026", "HP:0012120", "HP:0012343", "HP:0100660"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000608", "HP:0000750", "HP:0001249", "HP:0001250", "HP:0001254", "HP:0001257", "HP:0001332", "HP:0001347", "HP:0001510", "HP:0001522", "HP:0001945", "HP:0001974", "HP:0002059", "HP:0002329", "HP:0002360", "HP:0002500", "HP:0002813", "HP:0003819", "HP:0004353", "HP:0010551", "HP:0012127"], "RareDisease": ["OMIM:274270"], "Department": null}
{"Phenotype": ["HP:0000365", "HP:0000750", "HP:0001513", "HP:0001522", "HP:0001945", "HP:0003231", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000618", "HP:0000939", "HP:0001083", "HP:0001638", "HP:0001677", "HP:0001760", "HP:0002090", "HP:0002160", "HP:0003235", "HP:0003348", "HP:0003468", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:236200", "ORPHA:394", "CCRD:45"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001522", "HP:0003811", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000463", "HP:0000486", "HP:0000598", "HP:0001159", "HP:0001251", "HP:0001259", "HP:0001270", "HP:0001522", "HP:0001943", "HP:0003146", "HP:0003462", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0010569"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0001251", "HP:0001522", "HP:0003215", "HP:0003530", "HP:0003811", "HP:0003819", "HP:0008315", "HP:0100022"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000819", "HP:0002019", "HP:0040270"], "RareDisease": ["OMIM:125850", "ORPHA:552"], "Department": null}
{"Phenotype": ["HP:0000976", "HP:0000988", "HP:0001197", "HP:0001522", "HP:0002910", "HP:0003811", "HP:0010899", "HP:0010916", "HP:0010967", "HP:0100950"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0001629", "HP:0001638", "HP:0001974", "HP:0002013", "HP:0002098", "HP:0003075", "HP:0010472", "HP:0010899", "HP:0011968", "HP:0025435"], "RareDisease": ["OMIM:261750"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0010967"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001257", "HP:0001522", "HP:0002789", "HP:0008315", "HP:0012120", "HP:0040156", "HP:0045045"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001250", "HP:0001270", "HP:0001272", "HP:0001513", "HP:0001522", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0002151", "HP:0002179", "HP:0010899", "HP:0010916", "HP:0011968", "HP:0012714"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0001385", "HP:0001522", "HP:0001622", "HP:0003231", "HP:0003510", "HP:0003811", "HP:0004923", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001265", "HP:0001290", "HP:0003819", "HP:0004353", "HP:0012127"], "RareDisease": ["OMIM:222748"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001290", "HP:0001522", "HP:0001638", "HP:0001943", "HP:0002240", "HP:0002329", "HP:0002360", "HP:0003198", "HP:0008315", "HP:0012071"], "RareDisease": ["OMIM:201475", "ORPHA:26793", "CCRD:116"], "Department": null}
{"Phenotype": ["HP:0001513", "HP:0001522", "HP:0001875", "HP:0002149", "HP:0002151", "HP:0002240", "HP:0003811", "HP:0003819", "HP:0004429", "HP:0010899", "HP:0010916", "HP:0200039"], "RareDisease": ["OMIM:232220", "CCRD:35.2"], "Department": null}
{"Phenotype": ["HP:0000570", "HP:0000961", "HP:0001250", "HP:0001522", "HP:0002013", "HP:0002060", "HP:0002094", "HP:0003150", "HP:0011968"], "RareDisease": ["OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000077", "HP:0000822", "HP:0001250", "HP:0001259", "HP:0001522", "HP:0001638", "HP:0001873", "HP:0001882", "HP:0001903", "HP:0001974", "HP:0001987", "HP:0002013", "HP:0002149", "HP:0002151", "HP:0002152", "HP:0002153", "HP:0002154", "HP:0002155", "HP:0002652", "HP:0002789", "HP:0002912", "HP:0003075", "HP:0003124", "HP:0003138", "HP:0003155", "HP:0003165", "HP:0003210", "HP:0003228", "HP:0003235", "HP:0003259", "HP:0003348", "HP:0003510", "HP:0003811", "HP:0003819", "HP:0004421", "HP:0005117", "HP:0010472", "HP:0010906", "HP:0010910", "HP:0010967", "HP:0011421", "HP:0011966", "HP:0011968", "HP:0012026", "HP:0012120", "HP:0100613"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0000508", "HP:0000750", "HP:0001159", "HP:0001249", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0001760", "HP:0002705", "HP:0003462", "HP:0003819", "HP:0010569", "HP:0011421"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0001343", "HP:0001513", "HP:0001522", "HP:0001945", "HP:0003231", "HP:0003811", "HP:0004429", "HP:0004923", "HP:0011421", "HP:0040156"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0003215"], "RareDisease": ["OMIM:220110"], "Department": null}
{"Phenotype": ["HP:0001942", "HP:0003210", "HP:0003819"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0008315"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001522", "HP:0001987", "HP:0002013", "HP:0002329", "HP:0002360", "HP:0003218"], "RareDisease": ["OMIM:311250", "ORPHA:664", "CCRD:85"], "Department": null}
{"Phenotype": ["HP:0001522", "HP:0002659", "HP:0003811", "HP:0003819", "HP:0004923", "HP:0010917", "HP:0011421", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0000708", "HP:0000750", "HP:0000752", "HP:0001249", "HP:0001522", "HP:0003819", "HP:0004342"], "RareDisease": ["OMIM:230400", "ORPHA:79239", "CCRD:30"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001197", "HP:0001522", "HP:0003231", "HP:0003811", "HP:0003819", "HP:0004923"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0008315"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0001259", "HP:0001522", "HP:0001942", "HP:0001943", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0002151", "HP:0002919", "HP:0003819", "HP:0010895", "HP:0010967", "HP:0040156", "HP:0200039"], "RareDisease": ["OMIM:203750", "ORPHA:134", "CCRD:12"], "Department": null}
{"Phenotype": ["HP:0001051", "HP:0001250", "HP:0001290", "HP:0001522", "HP:0001942", "HP:0002151", "HP:0040156"], "RareDisease": ["OMIM:253260", "ORPHA:79241", "CCRD:13"], "Department": null}
{"Phenotype": ["HP:0003231", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001254", "HP:0001290", "HP:0001522", "HP:0001987", "HP:0002329", "HP:0002360", "HP:0003811", "HP:0011968", "HP:0500001"], "RareDisease": ["OMIM:248600", "ORPHA:511", "CCRD:67"], "Department": null}
{"Phenotype": ["HP:0000508", "HP:0000529", "HP:0000602", "HP:0001315", "HP:0003200", "HP:0003324", "HP:0003700", "HP:0200119", "HP:0200123"], "RareDisease": ["OMIM:251880"], "Department": null}
{"Phenotype": ["HP:0001942", "HP:0002013", "HP:0003819", "HP:0012120"], "RareDisease": ["OMIM:251000", "ORPHA:27", "CCRD:71"], "Department": null}
{"Phenotype": ["HP:0001596", "HP:0002013", "HP:0002014", "HP:0004923", "HP:0100613"], "RareDisease": ["OMIM:261600", "ORPHA:716", "CCRD:90"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001270", "HP:0001290", "HP:0001522", "HP:0002090", "HP:0002240", "HP:0008315", "HP:0040156"], "RareDisease": ["OMIM:271980", "ORPHA:22"], "Department": null}
{"Phenotype": ["HP:0001197", "HP:0001522", "HP:0003811", "HP:0003819", "HP:0004386", "HP:0008315"], "RareDisease": ["OMIM:201450", "ORPHA:42", "CCRD:70"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000639", "HP:0001249", "HP:0001251", "HP:0001265", "HP:0001270", "HP:0001272", "HP:0001290", "HP:0001298", "HP:0001510", "HP:0001522", "HP:0012642"], "RareDisease": ["OMIM:212065", "ORPHA:79318"], "Department": null}