FMO3

flavin containing monooxygenase 3
OMIM: 136132
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R98
Signed-off version 2.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Trimethylaminuria (Disorders and variants of enzymes that oxidise xenobiotics other than cytochrome P450)