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
ADPKD 4691
CVID14 54691
NS9 14691
polycystic kidney disease, autosomal dominant 4691
muscular dystrophy, congenital, 1c C564691
Noonan syndrome 9 14691
Noonan syndrome 9; NS9 http://purl.obolibrary.org/obo/MONDO_0014691
Noonan syndrome caused by mutation in SOS2 14691
Noonan syndrome type 9 14691
congenital, 1c muscular dystrophy C564691
SOS2 Noonan syndrome 14691
immunodeficiency, COMMON variable, 14 54691
immunodeficiency, common variable, 14 54691
immunodeficiency, COMMON variable, 14; CVID14 http://purl.obolibrary.org/obo/MONDO_0054691
congenital biliary ectasias 4691