Severe primary trimethylaminuria

Definition

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

Also identified as

• DOID 0080361 per MONDO
• MESH C536561 per MONDO
• OMIM 602079 per MONDO
• Orphanet 468726 per MONDO
• UMLS C5575503 per MONDO