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
EKV 17851
EKVP 17851
KTCN1 7851
Darier-Gottron disease 17851
Greither's disease 17851
keratoconus 1 7851
novak syndrome C537851
keratoconus type 1 7851
paroxysmal familial, 1 ventricular fibrillation C567851
erythrokeratodermia Figurata, congenital familial, 1N plaques http://purl.obolibrary.org/obo/MONDO_0017851
VSX1 keratoconus (disease) 7851
keratoconus 1; KTCN1 http://purl.obolibrary.org/obo/MONDO_0007851
erythrokeratodermia variabilis, Mendes da Costa type 17851
keratoconus (disease) caused by mutation in VSX1 7851
erythrokeratodermia variabilis ET progressiva 17851