Trimethylaminuria (TMAU)

Alias:

Tmau

Fish-Odor Syndrome

Severe Primary Trimethylaminuria

Fish Malodor Syndrome

Trimethylaminuria )

Stale Fish Syndrome

Fish Odour Syndrome

Fish Odor Syndrome

Mesh; D008661

Tmauria

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Trimethylaminuria, also known as tmau, is related to primary trimethylaminuria and albinism, oculocutaneous, type v. An important gene associated with Trimethylaminuria is FMO3 (Flavin Containing Dimethylaniline Monoxygenase 3), and among its related pathways/superpathways are Metabolism and Metapathway biotransformation Phase I and II. Affiliated tissues include liver and skin, and related phenotypes are fish odor and trimethylaminuria

Related ID：

MALACARDS：TRM004

OMIM：602079

MESH：C536561

ICD11：685690588