Severe primary trimethylaminuria

MONDO:0018767

Any trimethylaminuria in which the cause of the disease is a mutation in the FMO3 gene.

Also known as: trimethylaminuria, TMAU, TMAuria, fish malodor syndrome, fish odor syndrome, fish odour syndrome, fish-odor syndrome, stale fish syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Severe primary trimethylaminuria itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Trimethylaminuria (2)

Including sub-types (0) Tagged with Severe primary trimethylaminuria (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.