RareBench/LIRICAL.jsonl

{"Phenotype": ["HP:0000509", "HP:0001025", "HP:0001085", "HP:0002315", "HP:0002516", "HP:0002633", "HP:0003565", "HP:0011227", "HP:0011897"], "RareDisease": ["OMIM:191900", "ORPHA:575"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0001332", "HP:0002059", "HP:0003150", "HP:0100309"], "RareDisease": ["CCRD:34.1", "OMIM:231670", "ORPHA:25"], "Department": null}
{"Phenotype": ["HP:0000280", "HP:0000976", "HP:0001880", "HP:0002726", "HP:0003203", "HP:0003212", "HP:0006532", "HP:0011220", "HP:0025419", "HP:0031292", "HP:0031392", "HP:0031393"], "RareDisease": ["OMIM:147060", "ORPHA:2314"], "Department": null}
{"Phenotype": ["HP:0000272", "HP:0000405", "HP:0000470", "HP:0001014", "HP:0001251", "HP:0001256", "HP:0001433", "HP:0001650", "HP:0002071", "HP:0002779", "HP:0003355", "HP:0004322", "HP:0010729"], "RareDisease": ["OMIM:256540", "ORPHA:351"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000269", "HP:0000276", "HP:0000319", "HP:0000341", "HP:0000414", "HP:0000426", "HP:0000490", "HP:0000687", "HP:0000750", "HP:0000767", "HP:0001182", "HP:0001251", "HP:0002069", "HP:0002373", "HP:0010722", "HP:0011968", "HP:0012171", "HP:0100703"], "RareDisease": ["OMIM:614104", "ORPHA:464306"], "Department": null}
{"Phenotype": ["HP:0000076", "HP:0000308", "HP:0000733", "HP:0001252", "HP:0001263", "HP:0001266", "HP:0002136", "HP:0004209", "HP:0005709", "HP:0011968"], "RareDisease": ["OMIM:616973"], "Department": null}
{"Phenotype": ["HP:0000347", "HP:0000365", "HP:0000400", "HP:0000574", "HP:0000939", "HP:0002354", "HP:0002953", "HP:0004322", "HP:0004349", "HP:0009771", "HP:0011927", "HP:0012368"], "RareDisease": ["OMIM:102500", "ORPHA:955"], "Department": null}
{"Phenotype": ["HP:0000527", "HP:0000533", "HP:0000639", "HP:0000821", "HP:0000824", "HP:0001260", "HP:0001265", "HP:0001643", "HP:0001761", "HP:0002066", "HP:0002080", "HP:0002317", "HP:0003477", "HP:0004322", "HP:0006855", "HP:0008070", "HP:0011003"], "RareDisease": ["OMIM:275400", "ORPHA:3363"], "Department": null}
{"Phenotype": ["HP:0000331", "HP:0000377", "HP:0000498", "HP:0000577", "HP:0000582", "HP:0000767", "HP:0001263", "HP:0001363", "HP:0001385", "HP:0001508", "HP:0001880", "HP:0002155", "HP:0002652", "HP:0002812", "HP:0002938", "HP:0002943", "HP:0003416", "HP:0004430", "HP:0004565", "HP:0004566", "HP:0005352", "HP:0006610", "HP:0008445", "HP:0008947", "HP:0009826", "HP:0010605", "HP:0030043", "HP:0030320"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0001397", "HP:0001976", "HP:0003124", "HP:0003141", "HP:0003155", "HP:0010836", "HP:0010837", "HP:0012347", "HP:0012358", "HP:0031956", "HP:0031964"], "RareDisease": ["OMIM:616829", "ORPHA:466703"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0001324", "HP:0001371", "HP:0001385", "HP:0001611", "HP:0002136", "HP:0002650", "HP:0003390", "HP:0003557", "HP:0003803", "HP:0010831", "HP:0011968"], "RareDisease": ["OMIM:617146"], "Department": null}
{"Phenotype": ["HP:0000974", "HP:0000977", "HP:0001290", "HP:0001324", "HP:0001382", "HP:0002194", "HP:0002751", "HP:0031158"], "RareDisease": ["OMIM:130010"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000347", "HP:0000520", "HP:0000592", "HP:0000926", "HP:0000973", "HP:0001027", "HP:0001239", "HP:0001252", "HP:0001382", "HP:0001388", "HP:0001883", "HP:0002656", "HP:0002822", "HP:0002827", "HP:0002996", "HP:0003015", "HP:0004233", "HP:0004568", "HP:0006149", "HP:0006187", "HP:0006391", "HP:0008070", "HP:0009811", "HP:0011220", "HP:0011300", "HP:0011341", "HP:0012368", "HP:0100866"], "RareDisease": ["OMIM:271640", "ORPHA:93359"], "Department": null}
{"Phenotype": ["HP:0000059", "HP:0000248", "HP:0000252", "HP:0000322", "HP:0000341", "HP:0000378", "HP:0000455", "HP:0000463", "HP:0000482", "HP:0000490", "HP:0000527", "HP:0000565", "HP:0000574", "HP:0000664", "HP:0000878", "HP:0000938", "HP:0001263", "HP:0001511", "HP:0001643", "HP:0002000", "HP:0002020", "HP:0002205", "HP:0002553", "HP:0003196", "HP:0004209", "HP:0005709", "HP:0009907", "HP:0011800"], "RareDisease": ["OMIM:615502", "ORPHA:363611"], "Department": null}
{"Phenotype": ["HP:0000280", "HP:0000286", "HP:0000316", "HP:0000639", "HP:0001249", "HP:0001250", "HP:0001263", "HP:0001272", "HP:0001290", "HP:0001684", "HP:0002540", "HP:0002780", "HP:0002783", "HP:0003355", "HP:0005280", "HP:0008155", "HP:0010471", "HP:0040129"], "RareDisease": ["OMIM:616354", "ORPHA:397709"], "Department": null}
{"Phenotype": ["HP:0000083", "HP:0000243", "HP:0000369", "HP:0000568", "HP:0000601", "HP:0000656", "HP:0000695", "HP:0001433", "HP:0001508", "HP:0001511", "HP:0001763", "HP:0001788", "HP:0001873", "HP:0001875", "HP:0001888", "HP:0002013", "HP:0002021", "HP:0002090", "HP:0002148", "HP:0002901", "HP:0003073", "HP:0003075", "HP:0007431", "HP:0007479", "HP:0008064", "HP:0008689", "HP:0012472"], "RareDisease": ["OMIM:616395"], "Department": null}
{"Phenotype": ["HP:0000821", "HP:0001249", "HP:0001250", "HP:0001260", "HP:0001289", "HP:0001987", "HP:0002058", "HP:0002066", "HP:0002169", "HP:0002925", "HP:0003201", "HP:0003236", "HP:0005184", "HP:0006801", "HP:0007340", "HP:0009053"], "RareDisease": ["OMIM:616878", "ORPHA:480864"], "Department": null}
{"Phenotype": ["HP:0001132", "HP:0001519", "HP:0002647", "HP:0011003"], "RareDisease": ["OMIM:154700", "ORPHA:284963"], "Department": null}
{"Phenotype": ["HP:0000508", "HP:0000520", "HP:0002515", "HP:0002653", "HP:0002829", "HP:0003115", "HP:0003155", "HP:0003202", "HP:0003868", "HP:0011220", "HP:0012100", "HP:0100543", "HP:0100774"], "RareDisease": ["OMIM:131300", "ORPHA:1328"], "Department": null}
{"Phenotype": ["HP:0000340", "HP:0000414", "HP:0000496", "HP:0000582", "HP:0000750", "HP:0000964", "HP:0001249", "HP:0001250", "HP:0001290", "HP:0001344", "HP:0001558", "HP:0001562", "HP:0002099", "HP:0002283", "HP:0002376", "HP:0005946", "HP:0006829", "HP:0010804", "HP:0011344", "HP:0012444"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000194", "HP:0000248", "HP:0000340", "HP:0000343", "HP:0000490", "HP:0000565", "HP:0000586", "HP:0000817", "HP:0001270", "HP:0001344", "HP:0001347", "HP:0002421", "HP:0002878", "HP:0006829", "HP:0010804", "HP:0100716"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000212", "HP:0000737", "HP:0001371", "HP:0001824", "HP:0001941", "HP:0002153", "HP:0002243", "HP:0002902", "HP:0003073", "HP:0004395", "HP:0012531", "HP:0030350", "HP:0031359"], "RareDisease": ["OMIM:228600"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000704", "HP:0000974", "HP:0000978", "HP:0000993", "HP:0001027", "HP:0001030", "HP:0001058", "HP:0001249", "HP:0001270", "HP:0001319", "HP:0001537", "HP:0001582", "HP:0001763", "HP:0002619", "HP:0002643", "HP:0002650", "HP:0003419", "HP:0004417", "HP:0004419", "HP:0004976", "HP:0012432", "HP:0031158"], "RareDisease": ["OMIM:618000", "ORPHA:536532"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001252", "HP:0001263", "HP:0001315"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000498", "HP:0000613", "HP:0000653", "HP:0002231", "HP:0007431", "HP:0008070", "HP:0045075"], "RareDisease": ["OMIM:602400", "ORPHA:91132"], "Department": null}
{"Phenotype": ["HP:0000044", "HP:0001265", "HP:0001272", "HP:0002075", "HP:0007722", "HP:0030341", "HP:0030344", "HP:0040171"], "RareDisease": ["OMIM:215470", "ORPHA:1180"], "Department": null}
{"Phenotype": ["HP:0001276", "HP:0002011", "HP:0002107", "HP:0010946", "HP:0100660"], "RareDisease": ["OMIM:149400", "ORPHA:3197"], "Department": null}
{"Phenotype": ["HP:0000276", "HP:0000403", "HP:0000426", "HP:0000627", "HP:0001561", "HP:0001629", "HP:0002032", "HP:0002575", "HP:0002780", "HP:0003298", "HP:0011382", "HP:0031936", "HP:0100336", "HP:0100337"], "RareDisease": ["OMIM:214800", "ORPHA:138"], "Department": null}
{"Phenotype": ["HP:0000733", "HP:0001250", "HP:0001252", "HP:0002079", "HP:0002360", "HP:0003763", "HP:0005484", "HP:0007333", "HP:0008872"], "RareDisease": ["OMIM:613454"], "Department": null}
{"Phenotype": ["HP:0000518", "HP:0001300", "HP:0001761", "HP:0001765", "HP:0002174", "HP:0002355", "HP:0002460", "HP:0003200", "HP:0003688", "HP:0003693", "HP:0008619", "HP:0012049", "HP:0100660"], "RareDisease": ["OMIM:606324"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000032", "HP:0000049", "HP:0000054", "HP:0000271", "HP:0000316", "HP:0000324", "HP:0000356", "HP:0000358", "HP:0000369", "HP:0000448", "HP:0000478", "HP:0000708", "HP:0000729", "HP:0000965", "HP:0001249", "HP:0001250", "HP:0001252", "HP:0007772", "HP:0012683", "HP:0100764"], "RareDisease": ["OMIM:617516"], "Department": null}
{"Phenotype": ["HP:0000166", "HP:0000972", "HP:0006323", "HP:0011132", "HP:0025084", "HP:0410027"], "RareDisease": ["OMIM:245000", "ORPHA:678"], "Department": null}
{"Phenotype": ["HP:0000563", "HP:0001260", "HP:0001310", "HP:0002061", "HP:0002066", "HP:0002070", "HP:0006986"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0000020", "HP:0000716", "HP:0000738", "HP:0000741", "HP:0001268", "HP:0001289", "HP:0001332", "HP:0001350", "HP:0002015", "HP:0002059", "HP:0002167", "HP:0002172", "HP:0002527", "HP:0004326", "HP:0006801", "HP:0007256", "HP:0031825", "HP:0100660"], "RareDisease": ["OMIM:616840"], "Department": null}
{"Phenotype": ["HP:0001083", "HP:0001166", "HP:0001263", "HP:0001519"], "RareDisease": ["OMIM:236200", "ORPHA:394"], "Department": null}
{"Phenotype": ["HP:0000193", "HP:0000294", "HP:0000421", "HP:0000448", "HP:0000486", "HP:0000490", "HP:0000527", "HP:0000574", "HP:0000664", "HP:0000958", "HP:0000982", "HP:0001007", "HP:0001257", "HP:0001263", "HP:0001344", "HP:0002015", "HP:0002751", "HP:0006532", "HP:0006989"], "RareDisease": ["OMIM:609528", "ORPHA:66631"], "Department": null}
{"Phenotype": ["HP:0001257", "HP:0002011", "HP:0002359", "HP:0002754", "HP:0003487", "HP:0006801", "HP:0007021", "HP:0200042"], "RareDisease": ["OMIM:613115"], "Department": null}
{"Phenotype": ["HP:0001629", "HP:0001643", "HP:0001669", "HP:0001674", "HP:0001746", "HP:0001750", "HP:0002139", "HP:0003363", "HP:0004935", "HP:0004971", "HP:0012262", "HP:0012890"], "RareDisease": ["OMIM:306955"], "Department": null}
{"Phenotype": ["HP:0000958", "HP:0000980", "HP:0001155", "HP:0001760", "HP:0002209", "HP:0003777", "HP:0006482", "HP:0007401", "HP:0007502", "HP:0007663", "HP:0011509", "HP:0045075", "HP:0200040", "HP:0410400"], "RareDisease": ["OMIM:601553", "ORPHA:1573"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000252", "HP:0000286", "HP:0000347", "HP:0001249", "HP:0001270", "HP:0001276", "HP:0002360", "HP:0006956", "HP:0009879"], "RareDisease": ["OMIM:608716"], "Department": null}
{"Phenotype": ["HP:0000974", "HP:0000978", "HP:0001065", "HP:0001075", "HP:0001373", "HP:0001382", "HP:0001763", "HP:0002829", "HP:0025509"], "RareDisease": ["OMIM:130000", "ORPHA:287"], "Department": null}
{"Phenotype": ["HP:0000649", "HP:0000762", "HP:0001761", "HP:0002066", "HP:0002070", "HP:0002073", "HP:0002403", "HP:0003401", "HP:0003474", "HP:0007078", "HP:0007141", "HP:0009053", "HP:0031910", "HP:0100543"], "RareDisease": ["OMIM:601098", "ORPHA:101083"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000041", "HP:0000047", "HP:0000076", "HP:0000098", "HP:0000107", "HP:0000160", "HP:0000164", "HP:0000187", "HP:0000218", "HP:0000221", "HP:0000252", "HP:0000256", "HP:0000286", "HP:0000316", "HP:0000319", "HP:0000325", "HP:0000347", "HP:0000349", "HP:0000369", "HP:0000414", "HP:0000453", "HP:0000463", "HP:0000490", "HP:0000494", "HP:0000525", "HP:0000534", "HP:0000581", "HP:0000582", "HP:0000589", "HP:0000598", "HP:0000601", "HP:0000609", "HP:0000659", "HP:0000708", "HP:0000752", "HP:0000957", "HP:0000998", "HP:0001159", "HP:0001250", "HP:0001252", "HP:0001260", "HP:0001263", "HP:0001285", "HP:0001290", "HP:0001385", "HP:0001511", "HP:0001518", "HP:0001622", "HP:0001629", "HP:0001643", "HP:0001655", "HP:0001734", "HP:0001792", "HP:0002007", "HP:0002015", "HP:0002020", "HP:0002021", "HP:0002079", "HP:0002119", "HP:0002247", "HP:0002557", "HP:0002650", "HP:0002938", "HP:0003186", "HP:0003307", "HP:0004209", "HP:0004322", "HP:0004467", "HP:0004532", "HP:0006808", "HP:0007018", "HP:0008587", "HP:0010490", "HP:0010772", "HP:0011328", "HP:0011416", "HP:0011480", "HP:0012110", "HP:0012448", "HP:0012471", "HP:0012803", "HP:0025100", "HP:0030084", "HP:0030301", "HP:0045025", "HP:0200055", "HP:0410030"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0003281", "HP:0010836", "HP:0025435", "HP:0030890", "HP:0031956", "HP:0031964"], "RareDisease": ["OMIM:603553"], "Department": null}
{"Phenotype": ["HP:0000034", "HP:0000160", "HP:0000189", "HP:0000252", "HP:0000358", "HP:0000369", "HP:0000448", "HP:0000486", "HP:0000494", "HP:0000527", "HP:0000574", "HP:0000589", "HP:0000678", "HP:0000689", "HP:0000733", "HP:0000739", "HP:0000750", "HP:0001007", "HP:0001263", "HP:0002342", "HP:0002553", "HP:0002650", "HP:0009765", "HP:0010055", "HP:0011087", "HP:0011304"], "RareDisease": ["OMIM:613684", "ORPHA:353284"], "Department": null}
{"Phenotype": ["HP:0001268", "HP:0001350", "HP:0002510", "HP:0100660"], "RareDisease": ["OMIM:616840"], "Department": null}
{"Phenotype": ["HP:0001279", "HP:0001657", "HP:0001663", "HP:0001692", "HP:0001695", "HP:0004308", "HP:0011675", "HP:0031547"], "RareDisease": ["OMIM:614021"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001256", "HP:0001263", "HP:0001348", "HP:0001762", "HP:0002079", "HP:0002191", "HP:0002317", "HP:0006913", "HP:0008936", "HP:0011448", "HP:0012795", "HP:0030890"], "RareDisease": ["OMIM:613162", "ORPHA:320396"], "Department": null}
{"Phenotype": ["HP:0000010", "HP:0000467", "HP:0000969", "HP:0000988", "HP:0001263", "HP:0001270", "HP:0001284", "HP:0001324", "HP:0001558", "HP:0002829", "HP:0002907", "HP:0003115", "HP:0003458", "HP:0003687", "HP:0003724", "HP:0008944", "HP:0012587", "HP:0031910", "HP:0040083", "HP:0040129", "HP:0040180"], "RareDisease": ["OMIM:158810", "ORPHA:610"], "Department": null}
{"Phenotype": ["HP:0000248", "HP:0000486", "HP:0000520", "HP:0000586", "HP:0000826", "HP:0000954", "HP:0001250", "HP:0001263", "HP:0001845", "HP:0002069", "HP:0002353", "HP:0003186", "HP:0006191", "HP:0006543", "HP:0006829", "HP:0008947"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0001347", "HP:0003487", "HP:0006895", "HP:0040083"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0002980", "HP:0002984", "HP:0005736", "HP:0005792"], "RareDisease": ["OMIM:610915"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000577", "HP:0001249", "HP:0001250", "HP:0001260", "HP:0001943", "HP:0001987", "HP:0002058", "HP:0002104", "HP:0002373", "HP:0002376", "HP:0002913", "HP:0003201", "HP:0003236", "HP:0003487", "HP:0006801", "HP:0006957", "HP:0007359", "HP:0011675", "HP:0011675"], "RareDisease": ["OMIM:616878", "ORPHA:480864"], "Department": null}
{"Phenotype": ["HP:0000253", "HP:0000768", "HP:0000998", "HP:0001250", "HP:0001371", "HP:0001508", "HP:0001838", "HP:0002808", "HP:0003487", "HP:0005692", "HP:0007377", "HP:0007410", "HP:0009051", "HP:0011922", "HP:0012444", "HP:0012448", "HP:0012713"], "RareDisease": ["OMIM:617527", "ORPHA:521426"], "Department": null}
{"Phenotype": ["HP:0000365", "HP:0001249", "HP:0001250", "HP:0001263", "HP:0011318"], "RareDisease": ["OMIM:602849", "ORPHA:53271"], "Department": null}
{"Phenotype": ["HP:0000098", "HP:0000621", "HP:0000973", "HP:0001290", "HP:0001371", "HP:0001385", "HP:0001519", "HP:0001627", "HP:0001639", "HP:0001999", "HP:0002069", "HP:0002119", "HP:0002751", "HP:0004942"], "RareDisease": ["OMIM:617403"], "Department": null}
{"Phenotype": ["HP:0001663", "HP:0005184", "HP:0012819", "HP:0031677"], "RareDisease": ["OMIM:616247"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001371", "HP:0002380", "HP:0002515", "HP:0002650", "HP:0002875", "HP:0003202", "HP:0003323", "HP:0003327", "HP:0003391", "HP:0003473", "HP:0007911", "HP:0008944", "HP:0010535", "HP:0012473", "HP:0025331", "HP:0030208"], "RareDisease": ["OMIM:616325"], "Department": null}
{"Phenotype": ["HP:0000154", "HP:0000316", "HP:0000369", "HP:0000965", "HP:0001057", "HP:0001250", "HP:0001252", "HP:0001263", "HP:0001558", "HP:0002007", "HP:0002827", "HP:0005180", "HP:0005280", "HP:0006610", "HP:0011304", "HP:0200134"], "RareDisease": ["OMIM:608776", "ORPHA:79328"], "Department": null}
{"Phenotype": ["HP:0000238", "HP:0002119", "HP:0002507"], "RareDisease": ["OMIM:609637"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0001249", "HP:0001298", "HP:0002650", "HP:0003429"], "RareDisease": ["OMIM:617560", "ORPHA:527497"], "Department": null}
{"Phenotype": ["HP:0000926", "HP:0002515", "HP:0003015", "HP:0003183", "HP:0004568", "HP:0008802", "HP:0009381", "HP:0009826", "HP:0200055"], "RareDisease": ["OMIM:177170", "ORPHA:750"], "Department": null}
{"Phenotype": ["HP:0001268", "HP:0001761", "HP:0003128", "HP:0003259", "HP:0003326", "HP:0003393", "HP:0003394", "HP:0003546", "HP:0003760", "HP:0004305", "HP:0008954", "HP:0008959", "HP:0008981", "HP:0009130", "HP:0012378", "HP:0031177"], "RareDisease": ["OMIM:614321", "ORPHA:488650"], "Department": null}
{"Phenotype": ["HP:0000278", "HP:0000338", "HP:0000369", "HP:0001260", "HP:0001288", "HP:0001347", "HP:0002063", "HP:0002064", "HP:0002067", "HP:0004322", "HP:0025331", "HP:0100660"], "RareDisease": ["OMIM:606693", "ORPHA:306674"], "Department": null}
{"Phenotype": ["HP:0001230", "HP:0001249", "HP:0001831", "HP:0003038", "HP:0004322", "HP:0005736", "HP:0006009", "HP:0009381", "HP:0010049", "HP:0010055"], "RareDisease": ["OMIM:602875", "ORPHA:40"], "Department": null}
{"Phenotype": ["HP:0000518", "HP:0001251", "HP:0001263", "HP:0001272", "HP:0003417", "HP:0008820", "HP:0009901", "HP:0012368"], "RareDisease": ["OMIM:600373", "ORPHA:1458"], "Department": null}
{"Phenotype": ["HP:0000093", "HP:0001903", "HP:0100502"], "RareDisease": ["OMIM:261100", "ORPHA:35858"], "Department": null}
{"Phenotype": ["HP:0001433", "HP:0002716", "HP:0010701", "HP:0032455"], "RareDisease": ["OMIM:612840", "ORPHA:99844"], "Department": null}
{"Phenotype": ["HP:0000501", "HP:0000545", "HP:0001252", "HP:0001382", "HP:0002757", "HP:0003508", "HP:0007973", "HP:0030839", "HP:0030840"], "RareDisease": ["OMIM:604841", "ORPHA:90654"], "Department": null}
{"Phenotype": ["HP:0000787", "HP:0000869", "HP:0002315", "HP:0002588", "HP:0002893", "HP:0003165", "HP:0003418", "HP:0008200", "HP:0011748", "HP:0012587", "HP:0100522", "HP:0100570", "HP:0100634", "HP:0100829", "HP:0500167"], "RareDisease": ["OMIM:131100", "ORPHA:652"], "Department": null}
{"Phenotype": ["HP:0000083", "HP:0000107", "HP:0000252", "HP:0000961", "HP:0001338", "HP:0001522", "HP:0001629", "HP:0001660", "HP:0001671", "HP:0001845", "HP:0004935", "HP:0005301", "HP:0007430", "HP:0010442", "HP:0010773", "HP:0011611", "HP:0011662", "HP:0012020", "HP:0012050", "HP:0012516", "HP:0030148", "HP:0031664", "HP:0100520"], "RareDisease": ["OMIM:617478"], "Department": null}
{"Phenotype": ["HP:0001260", "HP:0001272", "HP:0002015", "HP:0002066", "HP:0002385", "HP:0002650", "HP:0011448"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0000514", "HP:0001260", "HP:0001276", "HP:0001285", "HP:0001776", "HP:0002070", "HP:0002317"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0000316", "HP:0000347", "HP:0000369", "HP:0000677", "HP:0000691", "HP:0000767", "HP:0001234", "HP:0001263", "HP:0001449", "HP:0002308", "HP:0002751", "HP:0003196", "HP:0010109", "HP:0011087", "HP:0012725", "HP:0030084"], "RareDisease": ["OMIM:605282", "ORPHA:363417"], "Department": null}
{"Phenotype": ["HP:0000098", "HP:0000119", "HP:0000621", "HP:0001290", "HP:0001371", "HP:0001385", "HP:0001519", "HP:0001522", "HP:0001627", "HP:0001639", "HP:0001999", "HP:0002751", "HP:0004942"], "RareDisease": ["OMIM:617402"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000490", "HP:0000519", "HP:0000958", "HP:0000992"], "RareDisease": ["OMIM:133540"], "Department": null}
{"Phenotype": ["HP:0000742", "HP:0001252", "HP:0001260", "HP:0001265", "HP:0001927", "HP:0002015", "HP:0002072", "HP:0003763", "HP:0006956"], "RareDisease": ["OMIM:200150", "ORPHA:2388"], "Department": null}
{"Phenotype": ["HP:0000582", "HP:0000601", "HP:0001263", "HP:0001387", "HP:0001642", "HP:0002938", "HP:0004322", "HP:0005164", "HP:0005280", "HP:0009803", "HP:0010579", "HP:0010884", "HP:0011800", "HP:0031027"], "RareDisease": ["OMIM:614185"], "Department": null}
{"Phenotype": ["HP:0002645", "HP:0002753", "HP:0002757", "HP:0002953", "HP:0003100", "HP:0003155", "HP:0031425", "HP:0031846", "HP:0040160"], "RareDisease": ["OMIM:615066"], "Department": null}
{"Phenotype": ["HP:0000733", "HP:0000750", "HP:0000817", "HP:0001250", "HP:0001252", "HP:0002079", "HP:0002353", "HP:0002360", "HP:0003763", "HP:0007333", "HP:0011968"], "RareDisease": ["OMIM:613454"], "Department": null}
{"Phenotype": ["HP:0000485", "HP:0000505", "HP:0007765", "HP:0012632"], "RareDisease": ["OMIM:309300", "ORPHA:91489"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0000952", "HP:0001290", "HP:0002013", "HP:0002069", "HP:0011968", "HP:0012024"], "RareDisease": ["OMIM:230400", "ORPHA:79239"], "Department": null}
{"Phenotype": ["HP:0000952", "HP:0001250", "HP:0001263", "HP:0001405", "HP:0001531", "HP:0001892", "HP:0001945", "HP:0002013", "HP:0002155", "HP:0002240", "HP:0002910", "HP:0003124", "HP:0003270", "HP:0004322"], "RareDisease": ["OMIM:232700", "ORPHA:369"], "Department": null}
{"Phenotype": ["HP:0000155", "HP:0000965", "HP:0001269", "HP:0001945", "HP:0002027", "HP:0002140", "HP:0002315", "HP:0002321", "HP:0002829", "HP:0003493", "HP:0010702", "HP:0011227", "HP:0012246"], "RareDisease": ["OMIM:615688", "ORPHA:404553"], "Department": null}
{"Phenotype": ["HP:0000126", "HP:0000260", "HP:0000280", "HP:0000316", "HP:0000341", "HP:0000369", "HP:0000885", "HP:0001098", "HP:0001141", "HP:0001250", "HP:0001263", "HP:0001510", "HP:0001540", "HP:0001561", "HP:0001643", "HP:0001655", "HP:0001762", "HP:0002007", "HP:0003270", "HP:0005280", "HP:0006487", "HP:0006956", "HP:0007082", "HP:0011129", "HP:0011800", "HP:0012714"], "RareDisease": ["OMIM:269150", "ORPHA:798"], "Department": null}
{"Phenotype": ["HP:0000537", "HP:0000635", "HP:0002226", "HP:0002227", "HP:0010862", "HP:0012453", "HP:0012745", "HP:0012785"], "RareDisease": ["OMIM:148820", "ORPHA:896"], "Department": null}
{"Phenotype": ["HP:0000054", "HP:0000212", "HP:0000343", "HP:0000347", "HP:0000463", "HP:0000520", "HP:0000892", "HP:0001647", "HP:0002007", "HP:0002937", "HP:0003042", "HP:0003086", "HP:0004322", "HP:0005280", "HP:0007655", "HP:0008551", "HP:0009381", "HP:0009826", "HP:0010281"], "RareDisease": ["OMIM:268310", "ORPHA:1507"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0001250", "HP:0001285", "HP:0001332", "HP:0001344", "HP:0002015", "HP:0002119", "HP:0002120", "HP:0002154", "HP:0002194", "HP:0002421", "HP:0002500", "HP:0003348", "HP:0004325", "HP:0012448", "HP:0031518"], "RareDisease": ["OMIM:617668"], "Department": null}
{"Phenotype": ["HP:0001822", "HP:0001847", "HP:0003155", "HP:0004363", "HP:0010064", "HP:0011987", "HP:0012531", "HP:0025021", "HP:0032436", "HP:0100529"], "RareDisease": ["OMIM:135100", "ORPHA:337"], "Department": null}
{"Phenotype": ["HP:0000277", "HP:0000508", "HP:0000544", "HP:0001771", "HP:0002486", "HP:0003693", "HP:0003722", "HP:0003749", "HP:0003749", "HP:0007209", "HP:0009053", "HP:0040129"], "RareDisease": ["OMIM:160150", "ORPHA:169189"], "Department": null}
{"Phenotype": ["HP:0000158", "HP:0000212", "HP:0000280", "HP:0000341", "HP:0000426", "HP:0000463", "HP:0000490", "HP:0000939", "HP:0001284", "HP:0001308", "HP:0001320", "HP:0001338", "HP:0002079", "HP:0002093", "HP:0002119", "HP:0002155", "HP:0002197", "HP:0002263", "HP:0002376", "HP:0002553", "HP:0002902", "HP:0006829", "HP:0007359", "HP:0011968", "HP:0012697", "HP:0012736", "HP:0100704"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000303", "HP:0000405", "HP:0000527", "HP:0001156", "HP:0001276", "HP:0001284", "HP:0001387", "HP:0001627", "HP:0002312", "HP:0002553", "HP:0002684", "HP:0002938", "HP:0002942", "HP:0004621", "HP:0008513", "HP:0012210", "HP:0012443", "HP:0032152"], "RareDisease": ["OMIM:139210", "ORPHA:2588"], "Department": null}
{"Phenotype": ["HP:0000325", "HP:0001629", "HP:0001631", "HP:0001643", "HP:0001875", "HP:0002308", "HP:0009778", "HP:0012506", "HP:0040012"], "RareDisease": ["OMIM:609053"], "Department": null}
{"Phenotype": ["HP:0000049", "HP:0000218", "HP:0000316", "HP:0000347", "HP:0000463", "HP:0000508", "HP:0001249", "HP:0001388", "HP:0001840", "HP:0004322"], "RareDisease": ["OMIM:305400", "ORPHA:915"], "Department": null}
{"Phenotype": ["HP:0000457", "HP:0000463", "HP:0000527", "HP:0000946", "HP:0001216", "HP:0001249", "HP:0001510", "HP:0002002", "HP:0002673", "HP:0002750", "HP:0002987", "HP:0003180", "HP:0003182", "HP:0004322", "HP:0008807", "HP:0008850", "HP:0012471"], "RareDisease": ["OMIM:102370", "ORPHA:969"], "Department": null}
{"Phenotype": ["HP:0001258", "HP:0001260", "HP:0002064", "HP:0002355", "HP:0002460", "HP:0002600", "HP:0007067"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000365", "HP:0000518", "HP:0000520", "HP:0001510"], "RareDisease": ["OMIM:216400"], "Department": null}
{"Phenotype": ["HP:0003341", "HP:0008066", "HP:0031446", "HP:0100806", "HP:0200041"], "RareDisease": ["OMIM:226700", "ORPHA:79404"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001324", "HP:0001344", "HP:0001649", "HP:0001664", "HP:0001695", "HP:0001943", "HP:0002151", "HP:0002913", "HP:0003201", "HP:0003236", "HP:0003324", "HP:0004756", "HP:0005184", "HP:0006543", "HP:0006956", "HP:0008942", "HP:0011675"], "RareDisease": ["OMIM:616878", "ORPHA:480864"], "Department": null}
{"Phenotype": ["HP:0001873", "HP:0011877", "HP:0012143", "HP:0030402", "HP:0032438"], "RareDisease": ["OMIM:615193"], "Department": null}
{"Phenotype": ["HP:0000268", "HP:0000483", "HP:0000486", "HP:0000508", "HP:0001065", "HP:0001166", "HP:0001519", "HP:0001653", "HP:0002647", "HP:0005180", "HP:0011003"], "RareDisease": ["OMIM:154700", "ORPHA:284963"], "Department": null}
{"Phenotype": ["HP:0000543", "HP:0000662", "HP:0007663", "HP:0007737", "HP:0007843"], "RareDisease": ["OMIM:600138"], "Department": null}
{"Phenotype": ["HP:0000635", "HP:0000639", "HP:0001010", "HP:0005599"], "RareDisease": ["OMIM:203200", "ORPHA:79432"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001263", "HP:0001290", "HP:0001999", "HP:0002750"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000639", "HP:0001252", "HP:0001257", "HP:0012736"], "RareDisease": ["OMIM:617560", "ORPHA:527497"], "Department": null}
{"Phenotype": ["HP:0000639", "HP:0002023", "HP:0002169", "HP:0002266", "HP:0002676", "HP:0004430", "HP:0007281", "HP:0025116"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000470", "HP:0000914", "HP:0001263", "HP:0001276", "HP:0001508", "HP:0001518", "HP:0001999", "HP:0002655", "HP:0002750", "HP:0002788", "HP:0002987", "HP:0003799", "HP:0004209", "HP:0004313", "HP:0004322", "HP:0005407", "HP:0005415", "HP:0005930", "HP:0009237", "HP:0009826", "HP:0011097", "HP:0011344", "HP:0011849", "HP:0025502", "HP:0031141"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000286", "HP:0000431", "HP:0000490", "HP:0000717", "HP:0000750", "HP:0001249", "HP:0001250", "HP:0001252", "HP:0001500", "HP:0001837", "HP:0002376", "HP:0002650", "HP:0007302", "HP:0011342"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0003557", "HP:0003701", "HP:0008180", "HP:0030319", "HP:0031237"], "RareDisease": ["OMIM:609200", "ORPHA:98911"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000252", "HP:0000278", "HP:0000286", "HP:0000331", "HP:0000341", "HP:0000463", "HP:0000508", "HP:0000574", "HP:0000664", "HP:0001007", "HP:0001508", "HP:0002194", "HP:0002553", "HP:0004209", "HP:0004691", "HP:0005280", "HP:0007665", "HP:0008872", "HP:0009623", "HP:0010044", "HP:0010047", "HP:0012210"], "RareDisease": ["OMIM:610759"], "Department": null}
{"Phenotype": ["HP:0000041", "HP:0000047", "HP:0000160", "HP:0000316", "HP:0000346", "HP:0000347", "HP:0000369", "HP:0000431", "HP:0001371", "HP:0001762", "HP:0005280", "HP:0008872", "HP:0100490"], "RareDisease": ["OMIM:193700", "ORPHA:2053"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000219", "HP:0000252", "HP:0000294", "HP:0000343", "HP:0000369", "HP:0000664", "HP:0000750", "HP:0000954", "HP:0001007", "HP:0005280", "HP:0007665", "HP:0008897", "HP:0010864"], "RareDisease": ["OMIM:122470", "ORPHA:199"], "Department": null}
{"Phenotype": ["HP:0002666", "HP:0003528", "HP:0025388"], "RareDisease": ["OMIM:171400", "ORPHA:247698"], "Department": null}
{"Phenotype": ["HP:0000023", "HP:0000243", "HP:0000252", "HP:0000280", "HP:0000520", "HP:0000768", "HP:0001357", "HP:0001371", "HP:0001508", "HP:0001518", "HP:0002194", "HP:0003307", "HP:0005280", "HP:0006801"], "RareDisease": ["OMIM:252500", "ORPHA:576"], "Department": null}
{"Phenotype": ["HP:0000248", "HP:0000316", "HP:0000341", "HP:0000520", "HP:0000750", "HP:0000768", "HP:0001156", "HP:0001561", "HP:0001561", "HP:0001822", "HP:0002020", "HP:0002098", "HP:0004209", "HP:0005280", "HP:0005469", "HP:0011951", "HP:0012471"], "RareDisease": ["OMIM:617180"], "Department": null}
{"Phenotype": ["HP:0000016", "HP:0000032", "HP:0000054", "HP:0000073", "HP:0000077", "HP:0000308", "HP:0000356", "HP:0000365", "HP:0000369", "HP:0000478", "HP:0000505", "HP:0000729", "HP:0000750", "HP:0000960", "HP:0001249", "HP:0001250", "HP:0001252", "HP:0001270", "HP:0001344", "HP:0001626", "HP:0001643", "HP:0002779", "HP:0002817", "HP:0003561", "HP:0008751", "HP:0009601", "HP:0010945", "HP:0011968", "HP:0012795", "HP:0100704"], "RareDisease": ["OMIM:617516"], "Department": null}
{"Phenotype": ["HP:0000470", "HP:0001249", "HP:0002751", "HP:0003418", "HP:0003422", "HP:0003521"], "RareDisease": ["OMIM:277300"], "Department": null}
{"Phenotype": ["HP:0000316", "HP:0001019", "HP:0001034", "HP:0001508", "HP:0002090", "HP:0002240", "HP:0003073", "HP:0004315", "HP:0005585", "HP:0006515", "HP:0006579", "HP:0011220", "HP:0030948", "HP:0032247", "HP:0040218", "HP:0410240", "HP:0410243"], "RareDisease": ["OMIM:222470", "ORPHA:84064"], "Department": null}
{"Phenotype": ["HP:0001873", "HP:0001892", "HP:0001902", "HP:0011871", "HP:0100309"], "RareDisease": ["OMIM:231200", "ORPHA:274"], "Department": null}
{"Phenotype": ["HP:0000270", "HP:0000689", "HP:0000696", "HP:0001388", "HP:0002645", "HP:0002866", "HP:0005280", "HP:0006660", "HP:0008788", "HP:0011069"], "RareDisease": ["OMIM:119600", "ORPHA:1452"], "Department": null}
{"Phenotype": ["HP:0000160", "HP:0000252", "HP:0000639", "HP:0000998", "HP:0001019", "HP:0001156", "HP:0001177", "HP:0001250", "HP:0001276", "HP:0001631", "HP:0001671", "HP:0001830", "HP:0001880", "HP:0001999", "HP:0002194", "HP:0002509", "HP:0002521", "HP:0002652", "HP:0002655", "HP:0002987", "HP:0004430", "HP:0004554", "HP:0005387", "HP:0005422", "HP:0008936", "HP:0012736", "HP:0040089", "HP:0100878"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0001433", "HP:0001903", "HP:0001945", "HP:0002113", "HP:0002716", "HP:0002788", "HP:0002851", "HP:0003237", "HP:0003261", "HP:0003270", "HP:0003496", "HP:0011897", "HP:0012311", "HP:0100827"], "RareDisease": ["OMIM:601859", "ORPHA:3261"], "Department": null}
{"Phenotype": ["HP:0000320", "HP:0000518", "HP:0000819", "HP:0000821", "HP:0000822", "HP:0000939", "HP:0000962", "HP:0001620", "HP:0001763", "HP:0001956", "HP:0002155", "HP:0002216", "HP:0003241", "HP:0003758", "HP:0004322", "HP:0005978", "HP:0012804", "HP:0025441"], "RareDisease": ["OMIM:277700", "ORPHA:902"], "Department": null}
{"Phenotype": ["HP:0000602", "HP:0001249", "HP:0001252", "HP:0001283", "HP:0001284", "HP:0002093", "HP:0002307", "HP:0002650", "HP:0003701", "HP:0006466"], "RareDisease": ["OMIM:161800"], "Department": null}
{"Phenotype": ["HP:0001252", "HP:0001263", "HP:0001290", "HP:0003124", "HP:0003141", "HP:0003155", "HP:0008947", "HP:0010837", "HP:0012347", "HP:0012358", "HP:0031956", "HP:0031964"], "RareDisease": ["OMIM:616829", "ORPHA:466703"], "Department": null}
{"Phenotype": ["HP:0000505", "HP:0000510", "HP:0000648", "HP:0000750", "HP:0001249", "HP:0001956", "HP:0007814", "HP:0007843", "HP:0010442", "HP:0030329"], "RareDisease": ["OMIM:615982"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000961", "HP:0000969", "HP:0001319", "HP:0001522", "HP:0001660", "HP:0001999", "HP:0003259", "HP:0004935", "HP:0005301", "HP:0007430", "HP:0010773", "HP:0011611", "HP:0011662", "HP:0012020", "HP:0012516", "HP:0030148", "HP:0031664", "HP:0031834"], "RareDisease": ["OMIM:617478"], "Department": null}
{"Phenotype": ["HP:0001635", "HP:0001644", "HP:0001678", "HP:0006699"], "RareDisease": ["OMIM:604145"], "Department": null}
{"Phenotype": ["HP:0000303", "HP:0000325", "HP:0000337", "HP:0000411", "HP:0000490", "HP:0000627", "HP:0000952", "HP:0000958", "HP:0001114", "HP:0001263", "HP:0001396", "HP:0002089", "HP:0002240", "HP:0003316", "HP:0011985", "HP:0012704", "HP:0030148", "HP:0045075"], "RareDisease": ["OMIM:118450", "ORPHA:52"], "Department": null}
{"Phenotype": ["HP:0000496", "HP:0001250", "HP:0001263", "HP:0007360", "HP:0007663"], "RareDisease": ["OMIM:617622"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000047", "HP:0000076", "HP:0000098", "HP:0000107", "HP:0000160", "HP:0000164", "HP:0000187", "HP:0000218", "HP:0000221", "HP:0000252", "HP:0000256", "HP:0000286", "HP:0000316", "HP:0000319", "HP:0000325", "HP:0000347", "HP:0000349", "HP:0000365", "HP:0000407", "HP:0000414", "HP:0000453", "HP:0000463", "HP:0000490", "HP:0000494", "HP:0000525", "HP:0000534", "HP:0000568", "HP:0000581", "HP:0000582", "HP:0000589", "HP:0000598", "HP:0000601", "HP:0000648", "HP:0000659", "HP:0000708", "HP:0000752", "HP:0000954", "HP:0000957", "HP:0000998", "HP:0001159", "HP:0001250", "HP:0001252", "HP:0001256", "HP:0001263", "HP:0001273", "HP:0001285", "HP:0001290", "HP:0001317", "HP:0001385", "HP:0001510", "HP:0001511", "HP:0001629", "HP:0001643", "HP:0001655", "HP:0001671", "HP:0001734", "HP:0001792", "HP:0002007", "HP:0002020", "HP:0002021", "HP:0002119", "HP:0002247", "HP:0002273", "HP:0002334", "HP:0002557", "HP:0002650", "HP:0002938", "HP:0003186", "HP:0003307", "HP:0003429", "HP:0004209", "HP:0004322", "HP:0004467", "HP:0004532", "HP:0006808", "HP:0007018", "HP:0007361", "HP:0010772", "HP:0011328", "HP:0011968", "HP:0012448", "HP:0012471", "HP:0025100", "HP:0030301", "HP:0045025", "HP:0200055", "HP:0410030"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000232", "HP:0000325", "HP:0000327", "HP:0000460", "HP:0000581", "HP:0000883", "HP:0000895", "HP:0001166", "HP:0001249", "HP:0001763", "HP:0002761", "HP:0002857", "HP:0002987", "HP:0003083", "HP:0005280", "HP:0012385"], "RareDisease": ["OMIM:600920", "ORPHA:2460"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000316", "HP:0000320", "HP:0000403", "HP:0000582", "HP:0001010", "HP:0001511", "HP:0002110", "HP:0002265", "HP:0002720", "HP:0002850", "HP:0003347", "HP:0003565", "HP:0004315", "HP:0006532", "HP:0011227", "HP:0030084", "HP:0032170"], "RareDisease": ["OMIM:251260", "ORPHA:647"], "Department": null}
{"Phenotype": ["HP:0000097", "HP:0000252", "HP:0000316", "HP:0000369", "HP:0000776", "HP:0002036", "HP:0002059", "HP:0002580", "HP:0008677", "HP:0009879"], "RareDisease": ["OMIM:617730"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000453", "HP:0002925", "HP:0008191", "HP:0011968", "HP:0031507", "HP:0100786"], "RareDisease": ["OMIM:241850", "ORPHA:1226"], "Department": null}
{"Phenotype": ["HP:0000274", "HP:0000336", "HP:0000486", "HP:0000586", "HP:0000706", "HP:0001006", "HP:0001596", "HP:0002007", "HP:0003510", "HP:0011120", "HP:0012471"], "RareDisease": ["OMIM:230740", "ORPHA:2067"], "Department": null}
{"Phenotype": ["HP:0000639", "HP:0001876", "HP:0002503", "HP:0002720", "HP:0002850", "HP:0004315", "HP:0005374", "HP:0005528", "HP:0007340", "HP:0008969"], "RareDisease": ["OMIM:159550", "ORPHA:2585"], "Department": null}
{"Phenotype": ["HP:0000164", "HP:0000561", "HP:0000971", "HP:0002223", "HP:0002298", "HP:0008404", "HP:0040039"], "RareDisease": ["OMIM:614931"], "Department": null}
{"Phenotype": ["HP:0000325", "HP:0000358", "HP:0000407", "HP:0000750", "HP:0001263", "HP:0001338", "HP:0001533", "HP:0002099", "HP:0004691", "HP:0010485", "HP:0045075", "HP:0045086", "HP:0100702"], "RareDisease": ["OMIM:604213", "ORPHA:314597"], "Department": null}
{"Phenotype": ["HP:0000193", "HP:0000272", "HP:0000347", "HP:0000768", "HP:0001166", "HP:0001631", "HP:0001655", "HP:0001659", "HP:0001704", "HP:0002616", "HP:0002650", "HP:0004927", "HP:0005180", "HP:0011645", "HP:0012385"], "RareDisease": ["OMIM:610168"], "Department": null}
{"Phenotype": ["HP:0000083", "HP:0000107", "HP:0001997", "HP:0002149", "HP:0003259", "HP:0003774"], "RareDisease": ["OMIM:162000", "ORPHA:88950"], "Department": null}
{"Phenotype": ["HP:0000239", "HP:0000242", "HP:0000680", "HP:0000774", "HP:0000894", "HP:0002007", "HP:0002645", "HP:0002650", "HP:0002866", "HP:0003396", "HP:0004322", "HP:0005259", "HP:0005280", "HP:0006297", "HP:0008788", "HP:0008804", "HP:0011223", "HP:0011800", "HP:0100864"], "RareDisease": ["OMIM:119600", "ORPHA:1452"], "Department": null}
{"Phenotype": ["HP:0000325", "HP:0000378", "HP:0000411", "HP:0000545", "HP:0000577", "HP:0000729", "HP:0001249", "HP:0001263", "HP:0004209", "HP:0005824", "HP:0008619", "HP:0009904", "HP:0100021"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0001288", "HP:0003044", "HP:0003273", "HP:0003798", "HP:0008994"], "RareDisease": ["OMIM:609285"], "Department": null}
{"Phenotype": ["HP:0000605", "HP:0000639", "HP:0001251", "HP:0001260", "HP:0001272", "HP:0002061", "HP:0002353", "HP:0002355", "HP:0002395", "HP:0003487", "HP:0007377", "HP:0012896", "HP:0100543"], "RareDisease": ["OMIM:607259", "ORPHA:99013"], "Department": null}
{"Phenotype": ["HP:0001257", "HP:0001260", "HP:0001272", "HP:0002015", "HP:0002066"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000054", "HP:0000308", "HP:0000376", "HP:0000480", "HP:0001290", "HP:0001635", "HP:0002015", "HP:0002020", "HP:0002033", "HP:0002643", "HP:0002878", "HP:0010628", "HP:0011381"], "RareDisease": ["OMIM:214800", "ORPHA:138"], "Department": null}
{"Phenotype": ["HP:0001347", "HP:0002061", "HP:0002497", "HP:0002506", "HP:0011448"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001324", "HP:0001433", "HP:0002376", "HP:0003236", "HP:0012759", "HP:0025435", "HP:0031956"], "RareDisease": ["OMIM:610217"], "Department": null}
{"Phenotype": ["HP:0000926", "HP:0001256", "HP:0001433", "HP:0002071", "HP:0008166", "HP:0010729"], "RareDisease": ["OMIM:230650", "ORPHA:79257"], "Department": null}
{"Phenotype": ["HP:0001595", "HP:0001597", "HP:0006482", "HP:0007530"], "RareDisease": ["OMIM:148600"], "Department": null}
{"Phenotype": ["HP:0000767", "HP:0000957", "HP:0001010", "HP:0001067", "HP:0001480", "HP:0002751", "HP:0007565", "HP:0009732"], "RareDisease": ["OMIM:162200", "ORPHA:363700"], "Department": null}
{"Phenotype": ["HP:0001397", "HP:0001405", "HP:0003124", "HP:0003155", "HP:0003236", "HP:0010837", "HP:0011967"], "RareDisease": ["OMIM:616829", "ORPHA:466703"], "Department": null}
{"Phenotype": ["HP:0000510", "HP:0000580", "HP:0000662", "HP:0001123", "HP:0007663", "HP:0007843", "HP:0012512", "HP:0025159"], "RareDisease": ["OMIM:617433"], "Department": null}
{"Phenotype": ["HP:0000543", "HP:0001257", "HP:0002015", "HP:0002194", "HP:0002300", "HP:0002421", "HP:0007663", "HP:0008947", "HP:0011471", "HP:0012043"], "RareDisease": ["OMIM:617560", "ORPHA:527497"], "Department": null}
{"Phenotype": ["HP:0000119", "HP:0000238", "HP:0001256", "HP:0001321", "HP:0001876", "HP:0002099", "HP:0002317", "HP:0002500", "HP:0002673", "HP:0004315", "HP:0031413", "HP:0100702"], "RareDisease": ["OMIM:159550", "ORPHA:2585"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001308", "HP:0001336", "HP:0002069", "HP:0002322", "HP:0002515", "HP:0003391", "HP:0003690", "HP:0003701", "HP:0010819", "HP:0012473", "HP:0040081", "HP:0045040"], "RareDisease": ["OMIM:159950", "ORPHA:2590"], "Department": null}
{"Phenotype": ["HP:0000280", "HP:0000486", "HP:0000767", "HP:0000886", "HP:0001252", "HP:0001270", "HP:0001407", "HP:0001539", "HP:0001582", "HP:0001653", "HP:0001999", "HP:0002176", "HP:0002651", "HP:0002673", "HP:0002751", "HP:0003048", "HP:0003090", "HP:0003265", "HP:0003319", "HP:0004322", "HP:0004565", "HP:0008462", "HP:0040163"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0004808", "HP:0012484", "HP:0030402"], "RareDisease": ["OMIM:601399"], "Department": null}
{"Phenotype": ["HP:0000347", "HP:0000508", "HP:0000822", "HP:0001284", "HP:0002938", "HP:0002987", "HP:0003077", "HP:0007485", "HP:0007495", "HP:0008112", "HP:0008994", "HP:0009046"], "RareDisease": ["OMIM:616516"], "Department": null}
{"Phenotype": ["HP:0000729", "HP:0000750", "HP:0001249", "HP:0001344", "HP:0010535", "HP:0010677"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001250", "HP:0001251", "HP:0001254", "HP:0001260", "HP:0001288", "HP:0001324", "HP:0001649", "HP:0001941", "HP:0001942", "HP:0001943", "HP:0001987", "HP:0002013", "HP:0002058", "HP:0002094", "HP:0002151", "HP:0002307", "HP:0002910", "HP:0002913", "HP:0002919", "HP:0003128", "HP:0003198", "HP:0003201", "HP:0003236", "HP:0003690", "HP:0004756", "HP:0005184", "HP:0006682", "HP:0006956", "HP:0007340", "HP:0012544", "HP:0045045", "HP:0100960"], "RareDisease": ["OMIM:616878", "ORPHA:480864"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000126", "HP:0000218", "HP:0000219", "HP:0000316", "HP:0000369", "HP:0000494", "HP:0000664", "HP:0000974", "HP:0001181", "HP:0001182", "HP:0001290", "HP:0001762", "HP:0002804", "HP:0006094", "HP:0010489"], "RareDisease": ["OMIM:601776", "ORPHA:2953"], "Department": null}
{"Phenotype": ["HP:0001258", "HP:0002064", "HP:0002355"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001257", "HP:0002064", "HP:0002169", "HP:0002312", "HP:0003401", "HP:0003487", "HP:0006886", "HP:0009830", "HP:0012534", "HP:0031910", "HP:0100543"], "RareDisease": ["OMIM:604187", "ORPHA:100991"], "Department": null}
{"Phenotype": ["HP:0000093", "HP:0000969", "HP:0001518", "HP:0002090", "HP:0002202", "HP:0003073", "HP:0003124", "HP:0008360", "HP:0008677"], "RareDisease": ["OMIM:256300", "ORPHA:839"], "Department": null}
{"Phenotype": ["HP:0000369", "HP:0000510", "HP:0000653", "HP:0000750", "HP:0000957", "HP:0001156", "HP:0004322", "HP:0008070", "HP:0009890", "HP:0012471", "HP:0031936", "HP:0045075"], "RareDisease": ["OMIM:250410", "ORPHA:166035"], "Department": null}
{"Phenotype": ["HP:0000158", "HP:0000262", "HP:0000280", "HP:0000341", "HP:0000426", "HP:0000463", "HP:0000490", "HP:0000565", "HP:0000648", "HP:0000878", "HP:0000998", "HP:0001250", "HP:0001284", "HP:0001320", "HP:0001338", "HP:0002079", "HP:0002119", "HP:0002263", "HP:0002353", "HP:0002376", "HP:0002553", "HP:0006829", "HP:0011968", "HP:0012020", "HP:0012697", "HP:0012736"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000316", "HP:0000337", "HP:0000369", "HP:0000470", "HP:0000475", "HP:0000494", "HP:0000957", "HP:0001480", "HP:0001488", "HP:0001510", "HP:0001638", "HP:0002162", "HP:0007018", "HP:0011968"], "RareDisease": ["OMIM:613224"], "Department": null}
{"Phenotype": ["HP:0000545", "HP:0000577", "HP:0001083", "HP:0001166", "HP:0001249", "HP:0001251", "HP:0001260", "HP:0001288", "HP:0007256", "HP:0012444", "HP:0030854", "HP:0031284"], "RareDisease": ["OMIM:236200", "ORPHA:394"], "Department": null}
{"Phenotype": ["HP:0000212", "HP:0000252", "HP:0000253", "HP:0000347", "HP:0000463", "HP:0000520", "HP:0000670", "HP:0000924", "HP:0000960", "HP:0001028", "HP:0001156", "HP:0001252", "HP:0001265", "HP:0001270", "HP:0001290", "HP:0001324", "HP:0001407", "HP:0001508", "HP:0001548", "HP:0001561", "HP:0002007", "HP:0002063", "HP:0002090", "HP:0002176", "HP:0002240", "HP:0002808", "HP:0002850", "HP:0002867", "HP:0002904", "HP:0002938", "HP:0003016", "HP:0003196", "HP:0003265", "HP:0003307", "HP:0003416", "HP:0003690", "HP:0004060", "HP:0004315", "HP:0004565", "HP:0005193", "HP:0005280", "HP:0005306", "HP:0005619", "HP:0006532", "HP:0007340", "HP:0008936", "HP:0009826", "HP:0100543", "HP:0100625", "HP:0100865"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0001761", "HP:0002527", "HP:0002921", "HP:0003448", "HP:0003487", "HP:0006970", "HP:0007340", "HP:0009072", "HP:0011808", "HP:0030180", "HP:0030181"], "RareDisease": ["OMIM:609260", "ORPHA:99947"], "Department": null}
{"Phenotype": ["HP:0000272", "HP:0000308", "HP:0000365", "HP:0000494"], "RareDisease": ["OMIM:613717"], "Department": null}
{"Phenotype": ["HP:0000161", "HP:0000252", "HP:0000437", "HP:0000873", "HP:0005273", "HP:0006870", "HP:0009099"], "RareDisease": ["OMIM:142946"], "Department": null}
{"Phenotype": ["HP:0000733", "HP:0000750", "HP:0001250", "HP:0001252", "HP:0002188", "HP:0002353", "HP:0002360", "HP:0005484", "HP:0008872"], "RareDisease": ["OMIM:613454"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000508", "HP:0000545", "HP:0000717", "HP:0000750", "HP:0000752", "HP:0001249", "HP:0004322", "HP:0005617", "HP:0010631", "HP:0031936"], "RareDisease": ["OMIM:617333"], "Department": null}
{"Phenotype": ["HP:0000023", "HP:0000076", "HP:0000579", "HP:0000670", "HP:0000822", "HP:0000973", "HP:0001653", "HP:0002110", "HP:0002616", "HP:0005180", "HP:0009926", "HP:0100857"], "RareDisease": ["OMIM:219100"], "Department": null}
{"Phenotype": ["HP:0000407", "HP:0000741", "HP:0002515", "HP:0002653", "HP:0003691", "HP:0003701", "HP:0003805", "HP:0007126", "HP:0008180", "HP:0010639", "HP:0100543"], "RareDisease": ["OMIM:167320", "ORPHA:52430"], "Department": null}
{"Phenotype": ["HP:0000394", "HP:0000506", "HP:0000556", "HP:0000813", "HP:0001153", "HP:0001642", "HP:0001647", "HP:0001770", "HP:0002023", "HP:0004209", "HP:0004322", "HP:0004442", "HP:0031624", "HP:0410049"], "RareDisease": ["OMIM:300707", "ORPHA:140952"], "Department": null}
{"Phenotype": ["HP:0000621", "HP:0000973", "HP:0001290", "HP:0001371", "HP:0001385", "HP:0001519", "HP:0001627", "HP:0001671", "HP:0001999", "HP:0002751", "HP:0007552"], "RareDisease": ["OMIM:617403"], "Department": null}
{"Phenotype": ["HP:0000158", "HP:0000252", "HP:0000280", "HP:0000527", "HP:0000664", "HP:0000824", "HP:0001007", "HP:0001250", "HP:0001265", "HP:0001270", "HP:0001344", "HP:0002120", "HP:0002376", "HP:0002650", "HP:0006829", "HP:0007957", "HP:0011344", "HP:0011734"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000319", "HP:0000343", "HP:0000347", "HP:0000365", "HP:0000518", "HP:0000527", "HP:0000670", "HP:0001252", "HP:0001270", "HP:0001488", "HP:0002007", "HP:0002205", "HP:0008872", "HP:0008897", "HP:0012646"], "RareDisease": ["OMIM:242840", "ORPHA:1493"], "Department": null}
{"Phenotype": ["HP:0001265", "HP:0001324", "HP:0002486", "HP:0003236", "HP:0003552", "HP:0003688", "HP:0003720"], "RareDisease": ["OMIM:160800"], "Department": null}
{"Phenotype": ["HP:0000952", "HP:0001744", "HP:0001903", "HP:0001923", "HP:0002240", "HP:0004445", "HP:0004844", "HP:0005560", "HP:0032106", "HP:0410177"], "RareDisease": ["OMIM:130600"], "Department": null}
{"Phenotype": ["HP:0001397", "HP:0001976", "HP:0002240", "HP:0003155", "HP:0010837", "HP:0011967"], "RareDisease": ["OMIM:616829", "ORPHA:466703"], "Department": null}
{"Phenotype": ["HP:0001260", "HP:0001283", "HP:0002015", "HP:0002273", "HP:0003487", "HP:0011448", "HP:0012473"], "RareDisease": ["OMIM:105400"], "Department": null}
{"Phenotype": ["HP:0000407", "HP:0001319", "HP:0001324", "HP:0001363", "HP:0001531", "HP:0002020", "HP:0002098", "HP:0002151", "HP:0002490", "HP:0002910", "HP:0003198", "HP:0003200", "HP:0003324", "HP:0003348", "HP:0003688", "HP:0008872", "HP:0011950", "HP:0045045"], "RareDisease": ["OMIM:616974", "ORPHA:478042"], "Department": null}
{"Phenotype": ["HP:0000952", "HP:0000989", "HP:0001396", "HP:0001433", "HP:0001510", "HP:0001627", "HP:0001928", "HP:0002240", "HP:0002650", "HP:0002908", "HP:0003112", "HP:0003573", "HP:0010701", "HP:0012202", "HP:0031956", "HP:0031964", "HP:0100810"], "RareDisease": ["OMIM:615878", "ORPHA:480483"], "Department": null}
{"Phenotype": ["HP:0000952", "HP:0001744", "HP:0001878", "HP:0001923", "HP:0005502"], "RareDisease": ["OMIM:612690"], "Department": null}
{"Phenotype": ["HP:0000047", "HP:0000369", "HP:0000508", "HP:0000589", "HP:0000609", "HP:0000612", "HP:0000819", "HP:0000822", "HP:0000961", "HP:0000969", "HP:0001290", "HP:0001488", "HP:0001561", "HP:0001629", "HP:0001631", "HP:0001635", "HP:0001655", "HP:0001671", "HP:0002003", "HP:0002094", "HP:0002104", "HP:0002119", "HP:0002282", "HP:0004502", "HP:0005133", "HP:0005280", "HP:0005989", "HP:0006610", "HP:0007700", "HP:0007957", "HP:0008551", "HP:0008936", "HP:0009062", "HP:0009800", "HP:0009879", "HP:0011220", "HP:0012785", "HP:0100598"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000341", "HP:0000426", "HP:0000463", "HP:0000490", "HP:0000505", "HP:0000939", "HP:0001250", "HP:0001284", "HP:0001320", "HP:0001347", "HP:0002079", "HP:0002093", "HP:0002119", "HP:0002263", "HP:0002353", "HP:0002376", "HP:0002380", "HP:0002553", "HP:0003477", "HP:0006829", "HP:0011968", "HP:0012697", "HP:0012736", "HP:0030236"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000365", "HP:0000592", "HP:0001371", "HP:0001433", "HP:0002757", "HP:0003116", "HP:0003155", "HP:0004322", "HP:0004349"], "RareDisease": ["OMIM:610968"], "Department": null}
{"Phenotype": ["HP:0000510", "HP:0000750", "HP:0000957", "HP:0001156", "HP:0001344", "HP:0001363", "HP:0001763", "HP:0001822", "HP:0002194", "HP:0004322", "HP:0007565"], "RareDisease": ["OMIM:250410", "ORPHA:166035"], "Department": null}
{"Phenotype": ["HP:0000280", "HP:0000349", "HP:0000403", "HP:0000414", "HP:0000729", "HP:0000739", "HP:0000750", "HP:0001156", "HP:0001212", "HP:0001263", "HP:0001992", "HP:0003112", "HP:0003355", "HP:0004322", "HP:0008155", "HP:0010471", "HP:0010529", "HP:0011893", "HP:0030352", "HP:0200055"], "RareDisease": ["OMIM:266265", "ORPHA:99843"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001987", "HP:0002181", "HP:0003218", "HP:0005961", "HP:0008358", "HP:0011966", "HP:0032397"], "RareDisease": ["OMIM:215700", "ORPHA:247525"], "Department": null}
{"Phenotype": ["HP:0000248", "HP:0000384", "HP:0000486", "HP:0000520", "HP:0000639", "HP:0000826", "HP:0000954", "HP:0001239", "HP:0001263", "HP:0001290", "HP:0001845", "HP:0002069", "HP:0002353", "HP:0002421", "HP:0002987", "HP:0003739", "HP:0006191", "HP:0006380", "HP:0006829", "HP:0007359", "HP:0008947"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000076", "HP:0000098", "HP:0000107", "HP:0000160", "HP:0000164", "HP:0000187", "HP:0000218", "HP:0000221", "HP:0000252", "HP:0000256", "HP:0000286", "HP:0000316", "HP:0000319", "HP:0000347", "HP:0000349", "HP:0000358", "HP:0000365", "HP:0000368", "HP:0000407", "HP:0000414", "HP:0000463", "HP:0000490", "HP:0000494", "HP:0000525", "HP:0000568", "HP:0000581", "HP:0000589", "HP:0000601", "HP:0000648", "HP:0000659", "HP:0000708", "HP:0000750", "HP:0000752", "HP:0000957", "HP:0000998", "HP:0001159", "HP:0001250", "HP:0001252", "HP:0001263", "HP:0001270", "HP:0001285", "HP:0001290", "HP:0001344", "HP:0001385", "HP:0001510", "HP:0001511", "HP:0001629", "HP:0001643", "HP:0001655", "HP:0001671", "HP:0001734", "HP:0001792", "HP:0002007", "HP:0002020", "HP:0002021", "HP:0002247", "HP:0002273", "HP:0002311", "HP:0002557", "HP:0002650", "HP:0002938", "HP:0003186", "HP:0003307", "HP:0004209", "HP:0004322", "HP:0004467", "HP:0004532", "HP:0007018", "HP:0011229", "HP:0011328", "HP:0011968", "HP:0012168", "HP:0012170", "HP:0012471", "HP:0045025", "HP:0200055", "HP:0200055", "HP:0410030"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0001250", "HP:0001259", "HP:0001263", "HP:0001344", "HP:0001664", "HP:0001943", "HP:0001946", "HP:0002061", "HP:0002133", "HP:0002151", "HP:0002913", "HP:0002919", "HP:0002925", "HP:0003128", "HP:0003201", "HP:0003236", "HP:0006846", "HP:0008936", "HP:0011675", "HP:0012444", "HP:0040145", "HP:0045045"], "RareDisease": ["OMIM:616878", "ORPHA:480864"], "Department": null}
{"Phenotype": ["HP:0001300", "HP:0002063", "HP:0002067", "HP:0002141", "HP:0002172", "HP:0002353", "HP:0002527"], "RareDisease": ["OMIM:260300", "ORPHA:171695"], "Department": null}
{"Phenotype": ["HP:0000044", "HP:0001029", "HP:0001875", "HP:0002110", "HP:0004322", "HP:0006530", "HP:0032252"], "RareDisease": ["OMIM:604173", "ORPHA:221046"], "Department": null}
{"Phenotype": ["HP:0000107", "HP:0000256", "HP:0000774", "HP:0001328", "HP:0002119", "HP:0002573", "HP:0009882", "HP:0011220", "HP:0030255"], "RareDisease": ["OMIM:616638", "ORPHA:457485"], "Department": null}
{"Phenotype": ["HP:0001627", "HP:0001972", "HP:0002011", "HP:0011873", "HP:0011893"], "RareDisease": ["CCRD:25", "OMIM:105650", "ORPHA:124"], "Department": null}
{"Phenotype": ["HP:0000518", "HP:0000790", "HP:0000829", "HP:0001281", "HP:0002024", "HP:0002321", "HP:0002728", "HP:0002901", "HP:0006297", "HP:0008207"], "RareDisease": ["OMIM:240300", "ORPHA:3453"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000218", "HP:0000239", "HP:0000248", "HP:0000368", "HP:0000494", "HP:0000520", "HP:0001561", "HP:0001631", "HP:0006610", "HP:0010709", "HP:0010713", "HP:0011220", "HP:0011800"], "RareDisease": ["OMIM:101200", "ORPHA:87"], "Department": null}
{"Phenotype": ["HP:0003074", "HP:0004904", "HP:0005562", "HP:0012090", "HP:0025329", "HP:0040217"], "RareDisease": ["OMIM:137920", "ORPHA:93111"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000467", "HP:0001249", "HP:0001324", "HP:0001623", "HP:0002747", "HP:0002751", "HP:0003391", "HP:0006380", "HP:0010546", "HP:0031936", "HP:0040129"], "RareDisease": ["OMIM:610687"], "Department": null}
{"Phenotype": ["HP:0001265", "HP:0001265", "HP:0001271", "HP:0003380", "HP:0003400", "HP:0005406", "HP:0007021", "HP:0011096", "HP:0012332", "HP:0030972", "HP:0031860", "HP:0031917", "HP:0040132"], "RareDisease": ["OMIM:201300"], "Department": null}
{"Phenotype": ["HP:0011897", "HP:0032434", "HP:0032435", "HP:0200042"], "RareDisease": ["OMIM:116920", "ORPHA:99842"], "Department": null}
{"Phenotype": ["HP:0000032", "HP:0000365", "HP:0000708", "HP:0000729", "HP:0000750", "HP:0001249", "HP:0001250", "HP:0001270", "HP:0001344", "HP:0001626", "HP:0011968", "HP:0030148"], "RareDisease": ["OMIM:617516"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000343", "HP:0000369", "HP:0000851", "HP:0001007", "HP:0001522", "HP:0001561", "HP:0002015", "HP:0002033", "HP:0002509", "HP:0002871", "HP:0003196", "HP:0007598", "HP:0007633", "HP:0008872", "HP:0008936", "HP:0010576", "HP:0011968", "HP:0025116", "HP:0031605", "HP:0100022", "HP:0100259"], "RareDisease": ["OMIM:617527", "ORPHA:521426"], "Department": null}
{"Phenotype": ["HP:0000790", "HP:0001385", "HP:0001903", "HP:0001942", "HP:0001974", "HP:0003159", "HP:0008672", "HP:0011227", "HP:0011280", "HP:0012085", "HP:0012100"], "RareDisease": ["OMIM:260000", "ORPHA:93599"], "Department": null}
{"Phenotype": ["HP:0000077", "HP:0000365", "HP:0000453", "HP:0000478", "HP:0000750", "HP:0000826", "HP:0001252", "HP:0001263", "HP:0001290", "HP:0001344", "HP:0001627", "HP:0002650", "HP:0007033", "HP:0010864", "HP:0011968", "HP:0025161"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0001252", "HP:0001290", "HP:0001382", "HP:0006443", "HP:0008404", "HP:0009781"], "RareDisease": ["OMIM:161200", "ORPHA:2614"], "Department": null}
{"Phenotype": ["HP:0000221", "HP:0000966", "HP:0000973", "HP:0003401", "HP:0003403", "HP:0007089"], "RareDisease": ["OMIM:105120", "ORPHA:85448"], "Department": null}
{"Phenotype": ["HP:0000343", "HP:0000400", "HP:0000414", "HP:0001649", "HP:0002069", "HP:0002104", "HP:0002536", "HP:0002719", "HP:0005957", "HP:0005972", "HP:0007204", "HP:0011294", "HP:0030917", "HP:0100259"], "RareDisease": ["OMIM:617527", "ORPHA:521426"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000510", "HP:0000608", "HP:0001263", "HP:0001328", "HP:0001513", "HP:0007843"], "RareDisease": ["OMIM:209900"], "Department": null}
{"Phenotype": ["HP:0000098", "HP:0000545", "HP:0000767", "HP:0000963", "HP:0001166", "HP:0001653", "HP:0002616", "HP:0002650", "HP:0002751", "HP:0004325", "HP:0012019"], "RareDisease": ["OMIM:154700", "ORPHA:284963"], "Department": null}
{"Phenotype": ["HP:0000233", "HP:0000260", "HP:0000316", "HP:0000347", "HP:0000369", "HP:0000463", "HP:0000470", "HP:0000474", "HP:0000582", "HP:0001239", "HP:0001274", "HP:0001305", "HP:0001511", "HP:0001627", "HP:0001942", "HP:0002002", "HP:0002119", "HP:0002335", "HP:0003196", "HP:0005280", "HP:0005684", "HP:0006380", "HP:0006466", "HP:0010880", "HP:0012210", "HP:0012385", "HP:0100806"], "RareDisease": ["OMIM:611182", "ORPHA:95428"], "Department": null}
{"Phenotype": ["HP:0000486", "HP:0000545", "HP:0000582", "HP:0000664", "HP:0000739", "HP:0000750", "HP:0001156", "HP:0001249", "HP:0001250", "HP:0001252", "HP:0001508", "HP:0001763", "HP:0001956", "HP:0002020", "HP:0002099", "HP:0002108", "HP:0002121", "HP:0002360", "HP:0002714", "HP:0004209", "HP:0004220", "HP:0004322", "HP:0011342", "HP:0012168", "HP:0100716"], "RareDisease": ["OMIM:182290", "ORPHA:819"], "Department": null}
{"Phenotype": ["HP:0000225", "HP:0000421", "HP:0000967", "HP:0001873", "HP:0004866", "HP:0008148", "HP:0011870", "HP:0011871", "HP:0011877", "HP:0012343"], "RareDisease": ["OMIM:231200", "ORPHA:274"], "Department": null}
{"Phenotype": ["HP:0001290", "HP:0001433", "HP:0001522", "HP:0001873", "HP:0003656", "HP:0004325", "HP:0007479"], "RareDisease": ["OMIM:608013", "ORPHA:85212"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000076", "HP:0000098", "HP:0000107", "HP:0000160", "HP:0000187", "HP:0000221", "HP:0000252", "HP:0000256", "HP:0000286", "HP:0000316", "HP:0000319", "HP:0000325", "HP:0000347", "HP:0000349", "HP:0000365", "HP:0000407", "HP:0000414", "HP:0000453", "HP:0000463", "HP:0000486", "HP:0000490", "HP:0000494", "HP:0000505", "HP:0000525", "HP:0000534", "HP:0000568", "HP:0000581", "HP:0000582", "HP:0000589", "HP:0000601", "HP:0000648", "HP:0000659", "HP:0000708", "HP:0000750", "HP:0000752", "HP:0000957", "HP:0000998", "HP:0001159", "HP:0001252", "HP:0001263", "HP:0001273", "HP:0001285", "HP:0001290", "HP:0001320", "HP:0001344", "HP:0001385", "HP:0001510", "HP:0001511", "HP:0001572", "HP:0001629", "HP:0001643", "HP:0001655", "HP:0001671", "HP:0001734", "HP:0001792", "HP:0001999", "HP:0002007", "HP:0002020", "HP:0002021", "HP:0002119", "HP:0002194", "HP:0002247", "HP:0002273", "HP:0002384", "HP:0002557", "HP:0002650", "HP:0002938", "HP:0003186", "HP:0003307", "HP:0003429", "HP:0004209", "HP:0004322", "HP:0004467", "HP:0004532", "HP:0006808", "HP:0007018", "HP:0007361", "HP:0010490", "HP:0010772", "HP:0011081", "HP:0011328", "HP:0011968", "HP:0012448", "HP:0012471", "HP:0025100", "HP:0030026", "HP:0030301", "HP:0045025", "HP:0100704", "HP:0200055", "HP:0410030"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0002099", "HP:0002750", "HP:0004322", "HP:0010535", "HP:0010862"], "RareDisease": ["OMIM:604804"], "Department": null}
{"Phenotype": ["HP:0000543", "HP:0001250", "HP:0001276", "HP:0001290", "HP:0001336", "HP:0001992", "HP:0002093", "HP:0002151", "HP:0002353", "HP:0002421", "HP:0003323", "HP:0006801", "HP:0006892", "HP:0007305", "HP:0011470", "HP:0025517", "HP:0031358", "HP:0100952"], "RareDisease": ["OMIM:616211"], "Department": null}
{"Phenotype": ["HP:0000233", "HP:0000325", "HP:0000369", "HP:0000460", "HP:0000592", "HP:0000963", "HP:0000973", "HP:0001075", "HP:0001263", "HP:0001382", "HP:0001385", "HP:0001763", "HP:0002194", "HP:0007392", "HP:0008887", "HP:0010648"], "RareDisease": ["OMIM:612940", "ORPHA:357064"], "Department": null}
{"Phenotype": ["HP:0000233", "HP:0000240", "HP:0000343", "HP:0001156", "HP:0001263", "HP:0001377", "HP:0001488", "HP:0001561", "HP:0002205", "HP:0002750", "HP:0003022", "HP:0003066", "HP:0003097", "HP:0004322", "HP:0009803", "HP:0010049"], "RareDisease": ["OMIM:231050"], "Department": null}
{"Phenotype": ["HP:0000020", "HP:0001258", "HP:0001260", "HP:0001348", "HP:0002064", "HP:0002355", "HP:0003487", "HP:0008081"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0000121", "HP:0000973", "HP:0001627", "HP:0001999"], "RareDisease": ["OMIM:617402"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000219", "HP:0000237", "HP:0000316", "HP:0000400", "HP:0000463", "HP:0000508", "HP:0001522", "HP:0002007", "HP:0005280", "HP:0010109", "HP:0010708", "HP:0010713", "HP:0011318", "HP:0011330", "HP:0011800"], "RareDisease": ["OMIM:101200", "ORPHA:87"], "Department": null}
{"Phenotype": ["HP:0000083", "HP:0000085", "HP:0000926", "HP:0001156", "HP:0001407", "HP:0001999", "HP:0002079", "HP:0002119", "HP:0002652", "HP:0002789", "HP:0005562", "HP:0009826", "HP:0011839", "HP:0030747"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0000238", "HP:0000256", "HP:0000316", "HP:0000369", "HP:0000470", "HP:0000486", "HP:0000508", "HP:0000767", "HP:0001250", "HP:0002967", "HP:0004322", "HP:0004482", "HP:0008070", "HP:0011342"], "RareDisease": ["OMIM:609942"], "Department": null}
{"Phenotype": ["HP:0000023", "HP:0000028", "HP:0000098", "HP:0000119", "HP:0000621", "HP:0000973", "HP:0001250", "HP:0001290", "HP:0001371", "HP:0001385", "HP:0001519", "HP:0001522", "HP:0001627", "HP:0001635", "HP:0001671", "HP:0001999", "HP:0002751", "HP:0004942", "HP:0007552"], "RareDisease": ["OMIM:617403"], "Department": null}
{"Phenotype": ["HP:0000077", "HP:0000316", "HP:0000357", "HP:0000365", "HP:0000385", "HP:0000395", "HP:0000408", "HP:0000431", "HP:0000453", "HP:0000567", "HP:0000589", "HP:0000612", "HP:0000708", "HP:0001249", "HP:0001250", "HP:0001252", "HP:0001263", "HP:0001290", "HP:0001344", "HP:0001371", "HP:0001385", "HP:0001510", "HP:0001511", "HP:0001649", "HP:0002098", "HP:0002355", "HP:0002376", "HP:0002650", "HP:0002944", "HP:0003698", "HP:0004322", "HP:0004384", "HP:0004502", "HP:0004755", "HP:0011849", "HP:0012368", "HP:0012803"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0004390", "HP:0032451", "HP:0032454"], "RareDisease": ["CCRD:89", "OMIM:175200", "ORPHA:2869"], "Department": null}
{"Phenotype": ["HP:0007556", "HP:0007559", "HP:0010765"], "RareDisease": ["OMIM:144200", "ORPHA:2199"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001263", "HP:0001276", "HP:0002188", "HP:0010851", "HP:0011167"], "RareDisease": ["OMIM:612164"], "Department": null}
{"Phenotype": ["HP:0001678", "HP:0001688", "HP:0005184", "HP:0030682"], "RareDisease": ["OMIM:616249"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000410", "HP:0000482", "HP:0000567", "HP:0000568", "HP:0000612", "HP:0000677", "HP:0000750", "HP:0001597", "HP:0004476", "HP:0007678", "HP:0008494", "HP:0012210"], "RareDisease": ["OMIM:113620", "ORPHA:1297"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0001263", "HP:0001270", "HP:0001344", "HP:0002353", "HP:0010864", "HP:0012443"], "RareDisease": ["OMIM:608393"], "Department": null}
{"Phenotype": ["HP:0000160", "HP:0000218", "HP:0000336", "HP:0000407", "HP:0000411", "HP:0000684", "HP:0000703", "HP:0002650", "HP:0002757", "HP:0004322", "HP:0004349", "HP:0004592", "HP:0005280", "HP:0011220", "HP:0011800", "HP:0045086"], "RareDisease": ["OMIM:613849"], "Department": null}
{"Phenotype": ["HP:0001284", "HP:0001761", "HP:0003431", "HP:0003448", "HP:0006937", "HP:0008959", "HP:0031810"], "RareDisease": ["OMIM:162500", "ORPHA:640"], "Department": null}
{"Phenotype": ["HP:0000635", "HP:0001100", "HP:0002226", "HP:0002227", "HP:0007894", "HP:0008527"], "RareDisease": ["OMIM:103500", "ORPHA:42665"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000047", "HP:0000076", "HP:0000098", "HP:0000107", "HP:0000160", "HP:0000164", "HP:0000187", "HP:0000218", "HP:0000221", "HP:0000252", "HP:0000256", "HP:0000286", "HP:0000316", "HP:0000319", "HP:0000325", "HP:0000347", "HP:0000349", "HP:0000365", "HP:0000407", "HP:0000414", "HP:0000453", "HP:0000463", "HP:0000490", "HP:0000494", "HP:0000525", "HP:0000534", "HP:0000568", "HP:0000581", "HP:0000582", "HP:0000589", "HP:0000598", "HP:0000601", "HP:0000648", "HP:0000659", "HP:0000708", "HP:0000717", "HP:0000750", "HP:0000752", "HP:0000957", "HP:0000998", "HP:0001159", "HP:0001249", "HP:0001250", "HP:0001252", "HP:0001273", "HP:0001285", "HP:0001290", "HP:0001344", "HP:0001385", "HP:0001510", "HP:0001511", "HP:0001629", "HP:0001643", "HP:0001655", "HP:0001671", "HP:0001734", "HP:0001792", "HP:0002007", "HP:0002015", "HP:0002020", "HP:0002021", "HP:0002247", "HP:0002273", "HP:0002557", "HP:0002650", "HP:0002938", "HP:0003186", "HP:0003307", "HP:0003429", "HP:0004209", "HP:0004322", "HP:0004467", "HP:0004532", "HP:0006808", "HP:0007018", "HP:0010490", "HP:0010772", "HP:0011328", "HP:0012448", "HP:0012471", "HP:0045025", "HP:0200055", "HP:0410030"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000107", "HP:0000126", "HP:0000154", "HP:0000252", "HP:0000331", "HP:0000400", "HP:0000414", "HP:0000486", "HP:0000582", "HP:0000952", "HP:0001252", "HP:0001263", "HP:0001558", "HP:0001591", "HP:0001792", "HP:0001883", "HP:0002000", "HP:0002098", "HP:0002236", "HP:0002944", "HP:0007099", "HP:0008689", "HP:0009890", "HP:0011819", "HP:0012385", "HP:0012450", "HP:0012523", "HP:0100730", "HP:0410018"], "RareDisease": ["OMIM:602342", "ORPHA:487825"], "Department": null}
{"Phenotype": ["HP:0000169", "HP:0009719", "HP:0009722", "HP:0009730"], "RareDisease": ["OMIM:613254"], "Department": null}
{"Phenotype": ["HP:0000239", "HP:0000242", "HP:0000316", "HP:0000680", "HP:0000774", "HP:0000894", "HP:0002007", "HP:0002645", "HP:0002650", "HP:0002866", "HP:0004322", "HP:0005259", "HP:0005280", "HP:0006297", "HP:0008788", "HP:0008804", "HP:0011223", "HP:0011800", "HP:0100864"], "RareDisease": ["OMIM:119600", "ORPHA:1452"], "Department": null}
{"Phenotype": ["HP:0000505", "HP:0000613", "HP:0000662", "HP:0001123"], "RareDisease": ["OMIM:120970", "ORPHA:1872"], "Department": null}
{"Phenotype": ["HP:0000365", "HP:0001319", "HP:0001410", "HP:0001531", "HP:0001712", "HP:0001941", "HP:0002033", "HP:0002098", "HP:0002126", "HP:0002151", "HP:0002490", "HP:0002910", "HP:0003128", "HP:0008872", "HP:0040288"], "RareDisease": ["OMIM:616974", "ORPHA:478042"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0001263", "HP:0001290", "HP:0001344", "HP:0011182"], "RareDisease": ["OMIM:614959"], "Department": null}
{"Phenotype": ["HP:0001663", "HP:0001688", "HP:0030682"], "RareDisease": ["OMIM:163800"], "Department": null}
{"Phenotype": ["HP:0000964", "HP:0001010", "HP:0001263", "HP:0001386", "HP:0001433", "HP:0001892", "HP:0001945", "HP:0002013", "HP:0002014", "HP:0002090", "HP:0003212", "HP:0004396", "HP:0008070", "HP:0012735"], "RareDisease": ["OMIM:214500", "ORPHA:167"], "Department": null}
{"Phenotype": ["HP:0000563", "HP:0001260", "HP:0001310", "HP:0002061", "HP:0002066", "HP:0002070", "HP:0006986"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0001762", "HP:0005792", "HP:0005855", "HP:0006385", "HP:0006487"], "RareDisease": ["OMIM:259440"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000365", "HP:0000648", "HP:0000750", "HP:0001263", "HP:0001332", "HP:0001508", "HP:0001943", "HP:0002120", "HP:0002307", "HP:0003128", "HP:0003200", "HP:0003535", "HP:0003688", "HP:0003781", "HP:0008936", "HP:0008947", "HP:0011968", "HP:0012157", "HP:0012707", "HP:0012708", "HP:0012751", "HP:0200134"], "RareDisease": ["OMIM:614739", "ORPHA:352328"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000574", "HP:0000689", "HP:0001162", "HP:0001212", "HP:0001250", "HP:0001263", "HP:0001511", "HP:0004209", "HP:0007236", "HP:0010554"], "RareDisease": ["OMIM:174300", "ORPHA:2919"], "Department": null}
{"Phenotype": ["HP:0001397", "HP:0001405", "HP:0003124", "HP:0003155", "HP:0003236", "HP:0010837", "HP:0011967"], "RareDisease": ["OMIM:616829", "ORPHA:466703"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000047", "HP:0000076", "HP:0000098", "HP:0000160", "HP:0000187", "HP:0000218", "HP:0000221", "HP:0000252", "HP:0000256", "HP:0000286", "HP:0000316", "HP:0000319", "HP:0000325", "HP:0000347", "HP:0000349", "HP:0000365", "HP:0000407", "HP:0000414", "HP:0000453", "HP:0000463", "HP:0000483", "HP:0000490", "HP:0000494", "HP:0000525", "HP:0000568", "HP:0000581", "HP:0000582", "HP:0000589", "HP:0000598", "HP:0000601", "HP:0000648", "HP:0000659", "HP:0000691", "HP:0000708", "HP:0000729", "HP:0000750", "HP:0000752", "HP:0000957", "HP:0000998", "HP:0001159", "HP:0001250", "HP:0001252", "HP:0001273", "HP:0001285", "HP:0001290", "HP:0001317", "HP:0001344", "HP:0001385", "HP:0001510", "HP:0001511", "HP:0001629", "HP:0001643", "HP:0001655", "HP:0001671", "HP:0001734", "HP:0001792", "HP:0002007", "HP:0002020", "HP:0002021", "HP:0002033", "HP:0002119", "HP:0002247", "HP:0002273", "HP:0002334", "HP:0002360", "HP:0002557", "HP:0002650", "HP:0002938", "HP:0003186", "HP:0003307", "HP:0003429", "HP:0004209", "HP:0004322", "HP:0004467", "HP:0004532", "HP:0006808", "HP:0007018", "HP:0007361", "HP:0010490", "HP:0010772", "HP:0010862", "HP:0011230", "HP:0011328", "HP:0011848", "HP:0011968", "HP:0012448", "HP:0012471", "HP:0025100", "HP:0030301", "HP:0045025", "HP:0200055", "HP:0410030"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000510", "HP:0000580", "HP:0000662", "HP:0001123", "HP:0007663", "HP:0007843", "HP:0012512", "HP:0025159"], "RareDisease": ["OMIM:617433"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000486", "HP:0000639", "HP:0001249", "HP:0001250", "HP:0001344", "HP:0002079", "HP:0002376", "HP:0002522", "HP:0006829", "HP:0006970", "HP:0011344"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000286", "HP:0000325", "HP:0000331", "HP:0000343", "HP:0000358", "HP:0000369", "HP:0000455", "HP:0000473", "HP:0000494", "HP:0000506", "HP:0000939", "HP:0001371", "HP:0001572", "HP:0002463", "HP:0002808", "HP:0005280", "HP:0006191", "HP:0011344", "HP:0100543", "HP:0200055"], "RareDisease": ["OMIM:617694"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000750", "HP:0001249", "HP:0001252", "HP:0001257", "HP:0001263", "HP:0002355"], "RareDisease": ["OMIM:614249"], "Department": null}
{"Phenotype": ["HP:0001371", "HP:0002104", "HP:0002540", "HP:0002792", "HP:0002793", "HP:0002878", "HP:0003202", "HP:0003388", "HP:0003691", "HP:0008959", "HP:0009027", "HP:0009053", "HP:0010307", "HP:0010535", "HP:0030210"], "RareDisease": ["OMIM:615120"], "Department": null}
{"Phenotype": ["HP:0000238", "HP:0001249", "HP:0002370", "HP:0002454", "HP:0003155", "HP:0003236", "HP:0012503"], "RareDisease": ["OMIM:234200", "ORPHA:157850"], "Department": null}
{"Phenotype": ["HP:0000077", "HP:0000154", "HP:0000316", "HP:0000453", "HP:0000463", "HP:0000664", "HP:0000708", "HP:0000722", "HP:0000729", "HP:0000733", "HP:0000739", "HP:0000750", "HP:0001263", "HP:0001627", "HP:0002360", "HP:0002474", "HP:0002650", "HP:0007015", "HP:0009889", "HP:0012372", "HP:0031468"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000752", "HP:0001249", "HP:0002750", "HP:0005338"], "RareDisease": ["OMIM:190350"], "Department": null}
{"Phenotype": ["HP:0000032", "HP:0000047", "HP:0000077", "HP:0000085", "HP:0000086", "HP:0000277", "HP:0000308", "HP:0000356", "HP:0000358", "HP:0000365", "HP:0000369", "HP:0000478", "HP:0000486", "HP:0000639", "HP:0000666", "HP:0000708", "HP:0000750", "HP:0001249", "HP:0001252", "HP:0001270", "HP:0001290", "HP:0001344", "HP:0001626", "HP:0001629", "HP:0001631", "HP:0001643", "HP:0001660", "HP:0002090", "HP:0002817", "HP:0004736", "HP:0006532", "HP:0009601", "HP:0011968", "HP:0012304"], "RareDisease": ["OMIM:617516"], "Department": null}
{"Phenotype": ["HP:0000543", "HP:0000649", "HP:0000666", "HP:0001257", "HP:0001332", "HP:0001583", "HP:0002300", "HP:0002421", "HP:0006958", "HP:0007015", "HP:0008947", "HP:0011471", "HP:0100543"], "RareDisease": ["OMIM:617560", "ORPHA:527497"], "Department": null}
{"Phenotype": ["HP:0001250", "HP:0009719", "HP:0009721", "HP:0010614", "HP:0012733", "HP:0012736", "HP:0100804"], "RareDisease": ["OMIM:191100"], "Department": null}
{"Phenotype": ["HP:0000365", "HP:0001662", "HP:0002789", "HP:0005184"], "RareDisease": ["OMIM:220400", "ORPHA:90647"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000054", "HP:0000252", "HP:0000280", "HP:0000316", "HP:0001935", "HP:0002669", "HP:0002714", "HP:0010864"], "RareDisease": ["OMIM:301040", "ORPHA:847"], "Department": null}
{"Phenotype": ["HP:0000160", "HP:0000252", "HP:0000358", "HP:0000448", "HP:0000486", "HP:0000494", "HP:0000527", "HP:0000574", "HP:0000589", "HP:0000678", "HP:0000689", "HP:0000729", "HP:0000739", "HP:0000750", "HP:0001007", "HP:0001263", "HP:0002342", "HP:0002553", "HP:0002650", "HP:0002750", "HP:0008872", "HP:0009765", "HP:0010055", "HP:0010562", "HP:0011087", "HP:0011304"], "RareDisease": ["OMIM:613684", "ORPHA:353284"], "Department": null}
{"Phenotype": ["HP:0000639", "HP:0000752", "HP:0001310", "HP:0001387", "HP:0001873", "HP:0001875", "HP:0002141", "HP:0002172", "HP:0002395", "HP:0002721", "HP:0002863", "HP:0007018", "HP:0011950"], "RareDisease": ["OMIM:159550", "ORPHA:2585"], "Department": null}
{"Phenotype": ["HP:0000023", "HP:0000952", "HP:0001263", "HP:0001397", "HP:0001507", "HP:0002904", "HP:0003124", "HP:0003141", "HP:0003155", "HP:0003236", "HP:0006579", "HP:0010837", "HP:0012347", "HP:0025321", "HP:0031956", "HP:0031964", "HP:0100790"], "RareDisease": ["OMIM:616829", "ORPHA:466703"], "Department": null}
{"Phenotype": ["HP:0000733", "HP:0000750", "HP:0001159", "HP:0001249", "HP:0001252", "HP:0001634", "HP:0001773", "HP:0002317", "HP:0031936"], "RareDisease": ["OMIM:615516", "ORPHA:329195"], "Department": null}
{"Phenotype": ["HP:0000164", "HP:0000316", "HP:0000369", "HP:0000456", "HP:0000494", "HP:0000508", "HP:0000912", "HP:0001156", "HP:0001233", "HP:0001274", "HP:0001328", "HP:0001363", "HP:0001807", "HP:0004209", "HP:0004440", "HP:0012741", "HP:0100874"], "RareDisease": ["OMIM:304110", "ORPHA:1520"], "Department": null}
{"Phenotype": ["HP:0000076", "HP:0000098", "HP:0000107", "HP:0000160", "HP:0000164", "HP:0000187", "HP:0000218", "HP:0000221", "HP:0000252", "HP:0000256", "HP:0000286", "HP:0000316", "HP:0000319", "HP:0000325", "HP:0000347", "HP:0000349", "HP:0000356", "HP:0000365", "HP:0000407", "HP:0000414", "HP:0000453", "HP:0000463", "HP:0000490", "HP:0000494", "HP:0000525", "HP:0000568", "HP:0000581", "HP:0000582", "HP:0000589", "HP:0000601", "HP:0000648", "HP:0000659", "HP:0000708", "HP:0000752", "HP:0000954", "HP:0000957", "HP:0000998", "HP:0001156", "HP:0001159", "HP:0001250", "HP:0001252", "HP:0001285", "HP:0001290", "HP:0001320", "HP:0001385", "HP:0001510", "HP:0001511", "HP:0001629", "HP:0001643", "HP:0001655", "HP:0001734", "HP:0001792", "HP:0001943", "HP:0001999", "HP:0002007", "HP:0002020", "HP:0002021", "HP:0002079", "HP:0002119", "HP:0002247", "HP:0002273", "HP:0002342", "HP:0002557", "HP:0002650", "HP:0002938", "HP:0003186", "HP:0003307", "HP:0003429", "HP:0004209", "HP:0004322", "HP:0004467", "HP:0004532", "HP:0005968", "HP:0006808", "HP:0007018", "HP:0007361", "HP:0010490", "HP:0010772", "HP:0011304", "HP:0011328", "HP:0011968", "HP:0012448", "HP:0012471", "HP:0030301", "HP:0045025", "HP:0200055", "HP:0410030"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000154", "HP:0000168", "HP:0000219", "HP:0000280", "HP:0000293", "HP:0000316", "HP:0000322", "HP:0000336", "HP:0000341", "HP:0000343", "HP:0000347", "HP:0000388", "HP:0000455", "HP:0000463", "HP:0000473", "HP:0000486", "HP:0000490", "HP:0000520", "HP:0000540", "HP:0000545", "HP:0000687", "HP:0000768", "HP:0001007", "HP:0001090", "HP:0001250", "HP:0001263", "HP:0001276", "HP:0001357", "HP:0001508", "HP:0001773", "HP:0002007", "HP:0002019", "HP:0002020", "HP:0002064", "HP:0002373", "HP:0002500", "HP:0002779", "HP:0003194", "HP:0003202", "HP:0003763", "HP:0004209", "HP:0004322", "HP:0005280", "HP:0005338", "HP:0006959", "HP:0007269", "HP:0009623", "HP:0009933", "HP:0010800", "HP:0012171", "HP:0012471", "HP:0200055", "HP:0430028"], "RareDisease": ["OMIM:617616", "ORPHA:513456"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000463", "HP:0000465", "HP:0000470", "HP:0000494", "HP:0000508", "HP:0000962", "HP:0001250", "HP:0001631", "HP:0001642", "HP:0004482", "HP:0005280", "HP:0008064", "HP:0008070", "HP:0009891", "HP:0010864"], "RareDisease": ["OMIM:115150", "ORPHA:1340"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000712", "HP:0000750", "HP:0001320", "HP:0001845", "HP:0002079", "HP:0002126", "HP:0004322", "HP:0004325", "HP:0012758"], "RareDisease": ["OMIM:614833", "ORPHA:468631"], "Department": null}
{"Phenotype": ["HP:0000750", "HP:0001263", "HP:0002069", "HP:0006821"], "RareDisease": ["OMIM:606854", "ORPHA:101070"], "Department": null}
{"Phenotype": ["HP:0000119", "HP:0000707", "HP:0001510", "HP:0001876", "HP:0002721", "HP:0005528", "HP:0031413"], "RareDisease": ["OMIM:159550", "ORPHA:2585"], "Department": null}
{"Phenotype": ["HP:0000662", "HP:0001123", "HP:0007663", "HP:0007737"], "RareDisease": ["OMIM:613750"], "Department": null}
{"Phenotype": ["HP:0000107", "HP:0000510", "HP:0000512", "HP:0000561", "HP:0000649", "HP:0001156", "HP:0001249", "HP:0001363", "HP:0001596", "HP:0002223", "HP:0004322", "HP:0008064", "HP:0011344", "HP:0011968"], "RareDisease": ["OMIM:250410", "ORPHA:166035"], "Department": null}
{"Phenotype": ["HP:0002322", "HP:0002451", "HP:0002527", "HP:0012332", "HP:0100543"], "RareDisease": ["OMIM:616840"], "Department": null}
{"Phenotype": ["HP:0000718", "HP:0000726", "HP:0002354"], "RareDisease": ["OMIM:606889"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000343", "HP:0000592", "HP:0000974", "HP:0000978", "HP:0001065", "HP:0001083", "HP:0001382", "HP:0001634", "HP:0002650", "HP:0005116", "HP:0010812", "HP:0012532", "HP:0100775", "HP:0100790"], "RareDisease": ["OMIM:614816"], "Department": null}
{"Phenotype": ["HP:0000639", "HP:0001251", "HP:0001260", "HP:0001903", "HP:0002066", "HP:0005528"], "RareDisease": ["OMIM:159550", "ORPHA:2585"], "Department": null}
{"Phenotype": ["HP:0000341", "HP:0000426", "HP:0000463", "HP:0000505", "HP:0001250", "HP:0001320", "HP:0002079", "HP:0002093", "HP:0002119", "HP:0002263", "HP:0002353", "HP:0002553", "HP:0003477", "HP:0011968", "HP:0012697", "HP:0012736"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000077", "HP:0000396", "HP:0000400", "HP:0000453", "HP:0000478", "HP:0000486", "HP:0000505", "HP:0000540", "HP:0000582", "HP:0000750", "HP:0000878", "HP:0001156", "HP:0001252", "HP:0001263", "HP:0001290", "HP:0001513", "HP:0001631", "HP:0001773", "HP:0002099", "HP:0002650", "HP:0002779", "HP:0002791", "HP:0004322", "HP:0004467", "HP:0007110", "HP:0012372", "HP:0012443", "HP:0030055", "HP:0100704", "HP:0200055", "HP:0400008"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000252", "HP:0000400", "HP:0000407", "HP:0000444", "HP:0000490", "HP:0000568", "HP:0001176", "HP:0001249", "HP:0001321", "HP:0002650", "HP:0002684", "HP:0002808", "HP:0003121", "HP:0004322", "HP:0005671", "HP:0008897", "HP:0011470"], "RareDisease": ["OMIM:133540"], "Department": null}
{"Phenotype": ["HP:0000733", "HP:0000750", "HP:0001250", "HP:0001252", "HP:0002079", "HP:0002188", "HP:0002353", "HP:0002376", "HP:0002540", "HP:0003763", "HP:0005484", "HP:0007333"], "RareDisease": ["OMIM:613454"], "Department": null}
{"Phenotype": ["HP:0000054", "HP:0000154", "HP:0000212", "HP:0000256", "HP:0000316", "HP:0000369", "HP:0000463", "HP:0000520", "HP:0000921", "HP:0002007", "HP:0002944", "HP:0002984", "HP:0003022", "HP:0003086", "HP:0004322", "HP:0005280", "HP:0008439", "HP:0010804", "HP:0012646", "HP:0200055"], "RareDisease": ["OMIM:268310", "ORPHA:1507"], "Department": null}
{"Phenotype": ["HP:0000047", "HP:0000048", "HP:0000054", "HP:0000062", "HP:0000369", "HP:0001047", "HP:0003146", "HP:0003196", "HP:0003462", "HP:0004691", "HP:0008734", "HP:0010569", "HP:0030087"], "RareDisease": ["OMIM:270400", "ORPHA:818"], "Department": null}
{"Phenotype": ["HP:0000135", "HP:0000486", "HP:0000543", "HP:0000662", "HP:0001513", "HP:0007663"], "RareDisease": ["OMIM:615983"], "Department": null}
{"Phenotype": ["HP:0000194", "HP:0000218", "HP:0000268", "HP:0000411", "HP:0000508", "HP:0000637", "HP:0000639", "HP:0001263", "HP:0001270", "HP:0001319", "HP:0001324", "HP:0001525", "HP:0001611", "HP:0002591", "HP:0002650", "HP:0003391", "HP:0010804", "HP:0030319"], "RareDisease": ["OMIM:616224"], "Department": null}
{"Phenotype": ["HP:0000119", "HP:0000621", "HP:0000973", "HP:0001290", "HP:0001371", "HP:0001385", "HP:0001519", "HP:0001627", "HP:0001999", "HP:0002107", "HP:0002617", "HP:0002751", "HP:0004942"], "RareDisease": ["OMIM:617402"], "Department": null}
{"Phenotype": ["HP:0001888", "HP:0002090", "HP:0002720", "HP:0030273", "HP:0031381", "HP:0032218"], "RareDisease": ["OMIM:102700", "ORPHA:277"], "Department": null}
{"Phenotype": ["HP:0000316", "HP:0000347", "HP:0000369", "HP:0000388", "HP:0000518", "HP:0000520", "HP:0000555", "HP:0000586", "HP:0000750", "HP:0001382", "HP:0001634", "HP:0002684", "HP:0002829", "HP:0003311", "HP:0004322", "HP:0006376", "HP:0008829", "HP:0011800", "HP:0410031"], "RareDisease": ["OMIM:108300", "ORPHA:90653"], "Department": null}
{"Phenotype": ["HP:0001880", "HP:0001888", "HP:0003212", "HP:0003237", "HP:0008404", "HP:0009098", "HP:0031392", "HP:0031393"], "RareDisease": ["OMIM:212050", "ORPHA:457088"], "Department": null}
{"Phenotype": ["HP:0000098", "HP:0001166", "HP:0002751", "HP:0009901", "HP:0012372", "HP:0012385"], "RareDisease": ["OMIM:121050", "ORPHA:115"], "Department": null}
{"Phenotype": ["HP:0000083", "HP:0000093", "HP:0000510", "HP:0000678", "HP:0000819", "HP:0001162", "HP:0001328", "HP:0001513", "HP:0100259"], "RareDisease": ["OMIM:615981"], "Department": null}
{"Phenotype": ["HP:0001519", "HP:0002650", "HP:0004970", "HP:0011003"], "RareDisease": ["OMIM:154700", "ORPHA:284963"], "Department": null}
{"Phenotype": ["HP:0001510", "HP:0001518", "HP:0001561", "HP:0003270", "HP:0005208", "HP:0012604", "HP:0032368", "HP:0032484", "HP:0032487"], "RareDisease": ["OMIM:616868"], "Department": null}
{"Phenotype": ["HP:0000065", "HP:0000105", "HP:0000138", "HP:0000388", "HP:0000842", "HP:0001263", "HP:0001712", "HP:0001943", "HP:0002035", "HP:0002090", "HP:0002719", "HP:0003270", "HP:0008665", "HP:0030796"], "RareDisease": ["OMIM:246200", "ORPHA:508"], "Department": null}
{"Phenotype": ["HP:0001249", "HP:0001250", "HP:0001263", "HP:0001290", "HP:0001508", "HP:0001942", "HP:0001943", "HP:0001946", "HP:0001987", "HP:0002013", "HP:0002098", "HP:0002151", "HP:0003201", "HP:0003648", "HP:0011675", "HP:0040145", "HP:0045045"], "RareDisease": ["OMIM:616878", "ORPHA:480864"], "Department": null}
{"Phenotype": ["HP:0000307", "HP:0000674", "HP:0000966", "HP:0001006", "HP:0001954", "HP:0005280", "HP:0009931", "HP:0011220", "HP:0012471"], "RareDisease": ["OMIM:305100", "ORPHA:181"], "Department": null}
{"Phenotype": ["HP:0000119", "HP:0000238", "HP:0001510", "HP:0001876", "HP:0002721", "HP:0005528", "HP:0100702"], "RareDisease": ["OMIM:159550", "ORPHA:2585"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000316", "HP:0000325", "HP:0000337", "HP:0000486", "HP:0000520", "HP:0000527", "HP:0000729", "HP:0000735", "HP:0000817", "HP:0000998", "HP:0001212", "HP:0001250", "HP:0001252", "HP:0001290", "HP:0001344", "HP:0001388", "HP:0001572", "HP:0002019", "HP:0002360", "HP:0002719", "HP:0004780", "HP:0008763", "HP:0011081", "HP:0011344", "HP:0100716"], "RareDisease": ["OMIM:618089"], "Department": null}
{"Phenotype": ["HP:0000194", "HP:0000303", "HP:0000337", "HP:0000365", "HP:0000414", "HP:0000708", "HP:0001290", "HP:0001344", "HP:0001999", "HP:0002376", "HP:0002750", "HP:0011344", "HP:0012471"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0001279", "HP:0001962", "HP:0012251"], "RareDisease": ["CCRD:14.3", "OMIM:601144", "ORPHA:130"], "Department": null}
{"Phenotype": ["HP:0000179", "HP:0000215", "HP:0000252", "HP:0000293", "HP:0000309", "HP:0000457", "HP:0000470", "HP:0000750", "HP:0000960", "HP:0001263", "HP:0001270", "HP:0003508", "HP:0007441", "HP:0008676", "HP:0010230", "HP:0011968"], "RareDisease": ["OMIM:605130", "ORPHA:319182"], "Department": null}
{"Phenotype": ["HP:0001019", "HP:0001263", "HP:0001347", "HP:0002179", "HP:0002197", "HP:0004322", "HP:0008873", "HP:0025116", "HP:0031430", "HP:0100806"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0000501", "HP:0000518", "HP:0001249", "HP:0001252", "HP:0003076", "HP:0003126", "HP:0003355", "HP:0012592"], "RareDisease": ["OMIM:309000", "ORPHA:534"], "Department": null}
{"Phenotype": ["HP:0000098", "HP:0000193", "HP:0000268", "HP:0000272", "HP:0000316", "HP:0000494", "HP:0000767", "HP:0001065", "HP:0001166", "HP:0001634", "HP:0002616", "HP:0002650", "HP:0003179", "HP:0004938", "HP:0010646", "HP:0011003", "HP:0012180", "HP:0100775"], "RareDisease": ["OMIM:609192", "ORPHA:60030"], "Department": null}
{"Phenotype": ["HP:0001156", "HP:0002970", "HP:0004060", "HP:0004379", "HP:0008450", "HP:0030352", "HP:0031508", "HP:0100864", "HP:0100866"], "RareDisease": ["OMIM:146000", "ORPHA:429"], "Department": null}
{"Phenotype": ["HP:0000726", "HP:0000738", "HP:0000746", "HP:0001260", "HP:0001288", "HP:0001300", "HP:0001332", "HP:0001337", "HP:0002063", "HP:0031908", "HP:0100660"], "RareDisease": ["OMIM:616840"], "Department": null}
{"Phenotype": ["HP:0000219", "HP:0000252", "HP:0000294", "HP:0000343", "HP:0000664", "HP:0000750", "HP:0002342", "HP:0005280", "HP:0007665", "HP:0008897"], "RareDisease": ["OMIM:122470", "ORPHA:199"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000269", "HP:0000567", "HP:0001531", "HP:0001944", "HP:0002013", "HP:0002014", "HP:0002902", "HP:0004325", "HP:0004467", "HP:0011106", "HP:0011470", "HP:0410030"], "RareDisease": ["OMIM:270420"], "Department": null}
{"Phenotype": ["HP:0000639", "HP:0001010", "HP:0005599"], "RareDisease": ["OMIM:203290", "ORPHA:79433"], "Department": null}
{"Phenotype": ["HP:0001251", "HP:0001260", "HP:0001272", "HP:0001310", "HP:0003487"], "RareDisease": ["OMIM:159550", "ORPHA:2585"], "Department": null}
{"Phenotype": ["HP:0000662", "HP:0001133", "HP:0007737", "HP:0008043"], "RareDisease": ["OMIM:601414"], "Department": null}
{"Phenotype": ["HP:0000010", "HP:0000077", "HP:0000286", "HP:0000294", "HP:0000316", "HP:0000341", "HP:0000453", "HP:0000476", "HP:0000664", "HP:0001252", "HP:0001257", "HP:0001270", "HP:0001276", "HP:0001290", "HP:0001627", "HP:0002194", "HP:0002650", "HP:0005989", "HP:0008589", "HP:0012372", "HP:0012443", "HP:0030680"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000508", "HP:0000592", "HP:0000703", "HP:0000926", "HP:0000938", "HP:0001249", "HP:0001270", "HP:0001510", "HP:0001788", "HP:0002757", "HP:0003023"], "RareDisease": ["OMIM:615220"], "Department": null}
{"Phenotype": ["HP:0000011", "HP:0000158", "HP:0000212", "HP:0000280", "HP:0000341", "HP:0000426", "HP:0000463", "HP:0000508", "HP:0000518", "HP:0000939", "HP:0001284", "HP:0001297", "HP:0001320", "HP:0001338", "HP:0002093", "HP:0002155", "HP:0002263", "HP:0002376", "HP:0002553", "HP:0006829", "HP:0007359", "HP:0010841", "HP:0011968", "HP:0012697", "HP:0012736", "HP:0100277", "HP:0100309", "HP:0100704"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0001257", "HP:0001260", "HP:0002066"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0000275", "HP:0000448", "HP:0000689", "HP:0000708", "HP:0001249", "HP:0006346", "HP:0011092", "HP:0040080", "HP:0100018"], "RareDisease": ["OMIM:302350", "ORPHA:627"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0001222", "HP:0001374", "HP:0001762", "HP:0002948", "HP:0003042", "HP:0003883", "HP:0004322", "HP:0005191", "HP:0008438", "HP:0011800", "HP:0011849"], "RareDisease": ["OMIM:150250", "ORPHA:503"], "Department": null}
{"Phenotype": ["HP:0000028", "HP:0000047", "HP:0000076", "HP:0000089", "HP:0000098", "HP:0000107", "HP:0000126", "HP:0000160", "HP:0000164", "HP:0000187", "HP:0000218", "HP:0000221", "HP:0000252", "HP:0000256", "HP:0000286", "HP:0000316", "HP:0000319", "HP:0000325", "HP:0000347", "HP:0000349", "HP:0000365", "HP:0000377", "HP:0000395", "HP:0000407", "HP:0000414", "HP:0000453", "HP:0000463", "HP:0000490", "HP:0000494", "HP:0000525", "HP:0000534", "HP:0000568", "HP:0000581", "HP:0000582", "HP:0000589", "HP:0000610", "HP:0000648", "HP:0000659", "HP:0000708", "HP:0000752", "HP:0000957", "HP:0001172", "HP:0001252", "HP:0001263", "HP:0001285", "HP:0001290", "HP:0001320", "HP:0001385", "HP:0001510", "HP:0001510", "HP:0001511", "HP:0001561", "HP:0001629", "HP:0001643", "HP:0001655", "HP:0001671", "HP:0001734", "HP:0001792", "HP:0001999", "HP:0002007", "HP:0002020", "HP:0002021", "HP:0002079", "HP:0002119", "HP:0002121", "HP:0002247", "HP:0002273", "HP:0002557", "HP:0002650", "HP:0002896", "HP:0002938", "HP:0003186", "HP:0003307", "HP:0003429", "HP:0004209", "HP:0004322", "HP:0004467", "HP:0006097", "HP:0006808", "HP:0007018", "HP:0007361", "HP:0007376", "HP:0008897", "HP:0009908", "HP:0010322", "HP:0010704", "HP:0010772", "HP:0011259", "HP:0011968", "HP:0012448", "HP:0012471", "HP:0025100", "HP:0030301", "HP:0045025", "HP:0200055", "HP:0410030"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0001156", "HP:0001387", "HP:0001642", "HP:0002650", "HP:0002938", "HP:0004322", "HP:0011003", "HP:0011623", "HP:0030961"], "RareDisease": ["OMIM:277600"], "Department": null}
{"Phenotype": ["HP:0000047", "HP:0000076", "HP:0000083", "HP:0000286", "HP:0000294", "HP:0000369", "HP:0000384", "HP:0000470", "HP:0000527", "HP:0000718", "HP:0000750", "HP:0000752", "HP:0001263", "HP:0001631", "HP:0001845", "HP:0002023", "HP:0002353", "HP:0004322", "HP:0007018", "HP:0008551", "HP:0009944", "HP:0012443", "HP:0100258"], "RareDisease": ["OMIM:107480"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000218", "HP:0000238", "HP:0000347", "HP:0000369", "HP:0000411", "HP:0000437", "HP:0000637", "HP:0001290", "HP:0001385", "HP:0001392", "HP:0001510", "HP:0001612", "HP:0001623", "HP:0001626", "HP:0001743", "HP:0006956", "HP:0007655", "HP:0008897", "HP:0031508", "HP:0045075"], "RareDisease": ["OMIM:300867"], "Department": null}
{"Phenotype": ["HP:0000212", "HP:0000218", "HP:0000276", "HP:0000365", "HP:0000486", "HP:0000666", "HP:0000678", "HP:0001238", "HP:0001263", "HP:0001285", "HP:0001290", "HP:0001321", "HP:0001332", "HP:0001347", "HP:0001548", "HP:0002079", "HP:0002415", "HP:0002500", "HP:0002650", "HP:0002828", "HP:0003429", "HP:0006808", "HP:0007034", "HP:0012444"], "RareDisease": ["OMIM:617560", "ORPHA:527497"], "Department": null}
{"Phenotype": ["HP:0000110", "HP:0000252", "HP:0000821", "HP:0000961", "HP:0000976", "HP:0001336", "HP:0001999", "HP:0002104", "HP:0002721", "HP:0002878", "HP:0002925", "HP:0003121", "HP:0005352", "HP:0005484", "HP:0005943", "HP:0008936", "HP:0010881", "HP:0011123", "HP:0012211", "HP:0031430"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0001878", "HP:0004444", "HP:0005502"], "RareDisease": ["OMIM:612653"], "Department": null}
{"Phenotype": ["HP:0000962", "HP:0001010", "HP:0001510", "HP:0002091", "HP:0002110", "HP:0002664", "HP:0002721", "HP:0002745", "HP:0007898", "HP:0008404", "HP:0031631", "HP:0100792"], "RareDisease": ["OMIM:613990"], "Department": null}
{"Phenotype": ["HP:0000729", "HP:0000750", "HP:0001250", "HP:0001263", "HP:0002018", "HP:0002019", "HP:0025051"], "RareDisease": ["OMIM:300352", "ORPHA:52503"], "Department": null}
{"Phenotype": ["HP:0000275", "HP:0000347", "HP:0000508", "HP:0000651", "HP:0001260", "HP:0001265", "HP:0002495", "HP:0002515", "HP:0002527", "HP:0002650", "HP:0002705", "HP:0002913", "HP:0003202", "HP:0003326", "HP:0003391", "HP:0003691", "HP:0003701", "HP:0009046", "HP:0010830", "HP:0040129"], "RareDisease": ["OMIM:609284"], "Department": null}
{"Phenotype": ["HP:0001258", "HP:0001260", "HP:0002066", "HP:0002070"], "RareDisease": ["OMIM:616907", "ORPHA:488594"], "Department": null}
{"Phenotype": ["HP:0000003", "HP:0000028", "HP:0000047", "HP:0000076", "HP:0000098", "HP:0000160", "HP:0000164", "HP:0000187", "HP:0000218", "HP:0000221", "HP:0000252", "HP:0000256", "HP:0000286", "HP:0000316", "HP:0000319", "HP:0000325", "HP:0000347", "HP:0000349", "HP:0000365", "HP:0000377", "HP:0000407", "HP:0000414", "HP:0000453", "HP:0000463", "HP:0000490", "HP:0000494", "HP:0000525", "HP:0000534", "HP:0000568", "HP:0000581", "HP:0000582", "HP:0000601", "HP:0000612", "HP:0000648", "HP:0000659", "HP:0000708", "HP:0000752", "HP:0000957", "HP:0000998", "HP:0001159", "HP:0001250", "HP:0001252", "HP:0001263", "HP:0001285", "HP:0001290", "HP:0001317", "HP:0001385", "HP:0001511", "HP:0001629", "HP:0001643", "HP:0001655", "HP:0001734", "HP:0001792", "HP:0002007", "HP:0002020", "HP:0002021", "HP:0002079", "HP:0002119", "HP:0002247", "HP:0002273", "HP:0002334", "HP:0002557", "HP:0002650", "HP:0002938", "HP:0003186", "HP:0003307", "HP:0004209", "HP:0004467", "HP:0004532", "HP:0006808", "HP:0007018", "HP:0007361", "HP:0008897", "HP:0010490", "HP:0010772", "HP:0011328", "HP:0011968", "HP:0012448", "HP:0012471", "HP:0025100", "HP:0030301", "HP:0045025", "HP:0200055", "HP:0410030"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0001873", "HP:0001892", "HP:0005513", "HP:0011974", "HP:0012528"], "RareDisease": ["OMIM:187900"], "Department": null}
{"Phenotype": ["HP:0001256", "HP:0002035", "HP:0003183", "HP:0003796", "HP:0008905", "HP:0010049", "HP:0010743"], "RareDisease": ["OMIM:223800", "ORPHA:239"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000316", "HP:0001623", "HP:0002650", "HP:0002827", "HP:0002947", "HP:0002987", "HP:0004976", "HP:0005280", "HP:0010049", "HP:0010301", "HP:0011432"], "RareDisease": ["OMIM:150250", "ORPHA:503"], "Department": null}
{"Phenotype": ["HP:0000253", "HP:0000322", "HP:0000486", "HP:0000574", "HP:0000580", "HP:0001182", "HP:0001263", "HP:0001290", "HP:0001317", "HP:0001382", "HP:0001510", "HP:0001956", "HP:0002033", "HP:0002363", "HP:0004322", "HP:0007074", "HP:0012471", "HP:0100874"], "RareDisease": ["OMIM:216550", "ORPHA:193"], "Department": null}
{"Phenotype": ["HP:0000518", "HP:0001263", "HP:0001266", "HP:0001270", "HP:0001290", "HP:0002023", "HP:0002059", "HP:0002061", "HP:0003112", "HP:0003542", "HP:0004322", "HP:0010818", "HP:0040081"], "RareDisease": ["OMIM:600373", "ORPHA:1458"], "Department": null}
{"Phenotype": ["HP:0000729", "HP:0001249", "HP:0001250", "HP:0001328", "HP:0009717", "HP:0009719", "HP:0010615"], "RareDisease": ["OMIM:191100"], "Department": null}
{"Phenotype": ["HP:0000218", "HP:0000219", "HP:0000276", "HP:0000319", "HP:0000337", "HP:0000400", "HP:0000490", "HP:0000508", "HP:0000601", "HP:0001511", "HP:0001636", "HP:0002020", "HP:0011968", "HP:0012758"], "RareDisease": ["OMIM:617452", "ORPHA:505237"], "Department": null}
{"Phenotype": ["HP:0000077", "HP:0000218", "HP:0000365", "HP:0000407", "HP:0000453", "HP:0000478", "HP:0000490", "HP:0000508", "HP:0000565", "HP:0000722", "HP:0000733", "HP:0000750", "HP:0000961", "HP:0001222", "HP:0001249", "HP:0001251", "HP:0001252", "HP:0001263", "HP:0001290", "HP:0001488", "HP:0001631", "HP:0001671", "HP:0001795", "HP:0002058", "HP:0002079", "HP:0002104", "HP:0002363", "HP:0002463", "HP:0002474", "HP:0002616", "HP:0002650", "HP:0003198", "HP:0010535", "HP:0012372", "HP:0030842"], "RareDisease": ["OMIM:616975"], "Department": null}
{"Phenotype": ["HP:0000248", "HP:0000365", "HP:0000403", "HP:0000486", "HP:0000750", "HP:0001249", "HP:0001263", "HP:0001270", "HP:0001290", "HP:0001956", "HP:0002360", "HP:0002650", "HP:0004322", "HP:0011800", "HP:0100716"], "RareDisease": ["OMIM:182290", "ORPHA:819"], "Department": null}
{"Phenotype": ["HP:0000473", "HP:0001270", "HP:0001302", "HP:0001336", "HP:0001339", "HP:0001347", "HP:0001385", "HP:0002069", "HP:0002174", "HP:0002857", "HP:0003307", "HP:0003487", "HP:0003808", "HP:0006956", "HP:0007018", "HP:0007033", "HP:0100021", "HP:0100543"], "RareDisease": ["OMIM:610031"], "Department": null}
{"Phenotype": ["HP:0001156", "HP:0001216", "HP:0001999", "HP:0002515", "HP:0002834", "HP:0002970", "HP:0003025", "HP:0003026", "HP:0003090", "HP:0003180", "HP:0004322", "HP:0004568", "HP:0008155", "HP:0008833", "HP:0008873", "HP:0010582", "HP:0012514"], "RareDisease": ["OMIM:177170", "ORPHA:750"], "Department": null}
{"Phenotype": ["HP:0000639", "HP:0001876", "HP:0005528"], "RareDisease": ["OMIM:159550", "ORPHA:2585"], "Department": null}
{"Phenotype": ["HP:0001279", "HP:0001638", "HP:0001663", "HP:0001695", "HP:0011712", "HP:0012819"], "RareDisease": ["CCRD:14.4", "OMIM:604772", "ORPHA:3286"], "Department": null}
{"Phenotype": ["HP:0000737", "HP:0001276", "HP:0001290", "HP:0001347", "HP:0001945", "HP:0006532"], "RareDisease": ["OMIM:245200", "ORPHA:487"], "Department": null}
{"Phenotype": ["HP:0000605", "HP:0001260", "HP:0001265", "HP:0002305"], "RareDisease": ["OMIM:208920", "ORPHA:1168"], "Department": null}
{"Phenotype": ["HP:0000407", "HP:0000848", "HP:0001252", "HP:0001561", "HP:0002149", "HP:0002150", "HP:0002902", "HP:0003113", "HP:0200114"], "RareDisease": ["OMIM:602522"], "Department": null}
{"Phenotype": ["HP:0000158", "HP:0000193", "HP:0001363", "HP:0001655", "HP:0001888", "HP:0001943", "HP:0001999", "HP:0002205", "HP:0002652", "HP:0002904", "HP:0008454", "HP:0011569"], "RareDisease": ["OMIM:617425"], "Department": null}
{"Phenotype": ["HP:0000967", "HP:0001873", "HP:0005537", "HP:0005548"], "RareDisease": ["OMIM:273900"], "Department": null}
{"Phenotype": ["HP:0000212", "HP:0000639", "HP:0001332", "HP:0002878", "HP:0006855", "HP:0007015", "HP:0007663", "HP:0008947", "HP:0100543"], "RareDisease": ["OMIM:617560", "ORPHA:527497"], "Department": null}
{"Phenotype": ["HP:0001433", "HP:0002180", "HP:0002354", "HP:0002361", "HP:0002448", "HP:0002527", "HP:0002529", "HP:0007009", "HP:0007017", "HP:0007064", "HP:0007086", "HP:0007164", "HP:0007272", "HP:0007369"], "RareDisease": ["CCRD:82.3", "OMIM:257220", "ORPHA:646"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000407", "HP:0000490", "HP:0000670", "HP:0000992", "HP:0001290", "HP:0004322"], "RareDisease": ["OMIM:216400"], "Department": null}
{"Phenotype": ["HP:0000340", "HP:0000414", "HP:0001249", "HP:0001250", "HP:0002283", "HP:0006829", "HP:0010804", "HP:0011344"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000011", "HP:0000158", "HP:0000256", "HP:0000280", "HP:0000574", "HP:0000836", "HP:0001249", "HP:0001250", "HP:0001315", "HP:0001344", "HP:0002376", "HP:0002650", "HP:0006829", "HP:0011344"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000301", "HP:0001283", "HP:0001371", "HP:0001388", "HP:0002505", "HP:0003236", "HP:0003691", "HP:0003720", "HP:0003749", "HP:0006520", "HP:0008994", "HP:0032178", "HP:0100851"], "RareDisease": ["OMIM:617232", "ORPHA:480682"], "Department": null}
{"Phenotype": ["HP:0000175", "HP:0000238", "HP:0000252", "HP:0000341", "HP:0000347", "HP:0000358", "HP:0000369", "HP:0000403", "HP:0000426", "HP:0000470", "HP:0000475", "HP:0000494", "HP:0000527", "HP:0000577", "HP:0000750", "HP:0000767", "HP:0000914", "HP:0001181", "HP:0001263", "HP:0001510", "HP:0001558", "HP:0001762", "HP:0001845", "HP:0002007", "HP:0002019", "HP:0002099", "HP:0002208", "HP:0002307", "HP:0003487", "HP:0005487", "HP:0006610", "HP:0007665", "HP:0031910", "HP:0100807"], "RareDisease": ["OMIM:602398", "ORPHA:35107"], "Department": null}
{"Phenotype": ["HP:0000325", "HP:0000957", "HP:0001371", "HP:0001511", "HP:0001629", "HP:0004322", "HP:0005528"], "RareDisease": ["OMIM:227645"], "Department": null}
{"Phenotype": ["HP:0000256", "HP:0000750", "HP:0001249", "HP:0001250", "HP:0001252", "HP:0001315", "HP:0001999", "HP:0002119", "HP:0002376", "HP:0011344"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000194", "HP:0000248", "HP:0000340", "HP:0000343", "HP:0000490", "HP:0000586", "HP:0000817", "HP:0001270", "HP:0001272", "HP:0001284", "HP:0001331", "HP:0001344", "HP:0001347", "HP:0001935", "HP:0002069", "HP:0002079", "HP:0002119", "HP:0002133", "HP:0002280", "HP:0002283", "HP:0002375", "HP:0002878", "HP:0005667", "HP:0006829", "HP:0007305", "HP:0010804", "HP:0011344", "HP:0012032", "HP:0012444", "HP:0100288"], "RareDisease": ["OMIM:616900", "ORPHA:488632"], "Department": null}
{"Phenotype": ["HP:0000473", "HP:0000511", "HP:0000571", "HP:0000605", "HP:0000639", "HP:0001251", "HP:0001260", "HP:0001270", "HP:0001272", "HP:0001332", "HP:0002062", "HP:0002497", "HP:0002540", "HP:0003429", "HP:0003474", "HP:0007108", "HP:0009830", "HP:0012547", "HP:0030187"], "RareDisease": ["OMIM:617560", "ORPHA:527497"], "Department": null}
{"Phenotype": ["HP:0000239", "HP:0000242", "HP:0000316", "HP:0000347", "HP:0000680", "HP:0000894", "HP:0002007", "HP:0002645", "HP:0002650", "HP:0002866", "HP:0004322", "HP:0005259", "HP:0005280", "HP:0006297", "HP:0008788", "HP:0008804", "HP:0011223", "HP:0011800", "HP:0100864"], "RareDisease": ["OMIM:119600", "ORPHA:1452"], "Department": null}
{"Phenotype": ["HP:0000252", "HP:0000485", "HP:0000543", "HP:0000639", "HP:0001263", "HP:0001272", "HP:0002079", "HP:0030890"], "RareDisease": ["OMIM:252650", "ORPHA:578"], "Department": null}