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Metadata
ID DOID:0080361
Name trimethylaminuria
Definition An inherited metabolic disorder characterized by the inability 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://www.genome.gov/Genetic-Disorders/Trimethylaminuria, https://ghr.nlm.nih.gov/condition/trimethylaminuria
Xrefs

GARD:6447

MESH:C536561

MIM:602079

ORDO:468726

Subsets

DO_rare_slim

Synonyms

fish-odor syndrome [EXACT]

Parent Relationships

is_a inherited metabolic disorder

is_a autosomal recessive disease

Subclass Logical Relationships

has material basis in some autosomal recessive inheritance

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