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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