MONDO_merge Find_IDs Find_Terms Annotation
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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
gingival fibromatosis, 3 12378
noonan syndrome 3 C537847
posterior polymorphous, 3 corneal dystrophy C563788
deficiency of 3-beta-hydroxysteroid-delta(5)-desaturase C537880
fibromatosis, gingival, 3; GINGF3 http://purl.obolibrary.org/obo/MONDO_0012378
deafness, X-linked 5 10378
deafness, X-linked 5; DFNX5 http://purl.obolibrary.org/obo/MONDO_0010378
retinitis pigmentosa 63 13780
retinitis pigmentosa 63; RP63 http://purl.obolibrary.org/obo/MONDO_0013780
retinitis pigmentosa 64 13786
partial trisomy 6q chromosome 6 C537810
partial trisomy 6q syndrome C537810
monosomy chromosome 7 C537814
ring chromosome 7 syndrome C537813
partial monosomy 7p chromosome 7 C537818