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Metadata
ID DOID:0080361
Name trimethylaminuria
Definition An inherited metabolic disorder characterized by the inabilty to break down trimethylamine and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding flavin-containing monooxygenase-3 on chromosome 1q24.
https://ghr.nlm.nih.gov/condition/trimethylaminuria
Xrefs

GARD:6447

MESH:C536561

OMIM:602079

ORDO:468726

Synonyms

fish-odor syndrome [EXACT]

Parent Relationships

is_a inherited metabolic disorder

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