Disease Term Disease ID Gene Symbol Classification References Source
NON RARE IN EUROPE: Trimethylaminuria 35056 FMO3 Causal Pathogenic evidence from ClinVar - ClinVar
Severe primary trimethylaminuria 468726 FMO3 Causal Pathogenic evidence from ClinVar - ClinVar
Trimethylaminuria C0342739 FMO3 Causal Pathogenic evidence from ClinVar 9282831, 9398858, 9536088, 10338091, 10479479, 11191884, 12214664, 12893987, 16601883, 16996766, 17531949, 17584019, 19321370, 21451776, 23791655, 28392825, 28649550, 28743400 ClinVar