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
OI type 10 13459
constitutional megaloblastic anemia with severe neurologic disease 13456
OI type X 13459
Leber congenital amaurosis 11 13454
Leber congenital amaurosis 11; LCA11 http://purl.obolibrary.org/obo/MONDO_0013454
Leber congenital amaurosis 15 13457
Leber congenital amaurosis 15; LCA15 http://purl.obolibrary.org/obo/MONDO_0013457
Leber congenital amaurosis 8 13453
Leber congenital amaurosis 8; LCA8 http://purl.obolibrary.org/obo/MONDO_0013453
Leber congenital amaurosis caused by mutation in CRB1 13453
Leber congenital amaurosis caused by mutation in IMPDH1 13454
Leber congenital amaurosis caused by mutation in TULP1 13457
Leber congenital amaurosis type 11 13454
Leber congenital amaurosis type 15 13457
Leber congenital amaurosis type 8 13453