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
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4 13156
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4; MDDGB4 http://purl.obolibrary.org/obo/MONDO_0013156
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B4 13156.0
disease, splenic D013158
diseases, splenic D013158
splenic diseases D013158
infarct, splenic D013159
infarction, splenic D013159
infarctions, splenic D013159
infarcts, splenic D013159
splenic infarctions D013159
muscular dystrophy, congenital, Fktn-Related http://purl.obolibrary.org/obo/MONDO_0013156
IL10RA inflammatory bowel disease 13153
choroidal dystrophy, central areolar, 3 13151
choroidal dystrophy, central areolar, 3; CACD3 http://purl.obolibrary.org/obo/MONDO_0013151