Severe primary trimethylaminuria

disorder

SNOMED 1237339005CUI C5575503

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Fishy odor

Always present (100%)HP:0410020

High urine trimethylamine levels

Very frequent (80-99%)HP:0003614

Emotional lability

Frequent (30-79%)HP:0000712

Low self-esteem

Frequent (30-79%)HP:0031469

Neuroticism

Frequent (30-79%)HP:0031467

Anxiety disease

Occasional (5-29%)HP:0000739

Depressive episode

Occasional (5-29%)HP:0000716

Obsessive-compulsive trait

Occasional (5-29%)HP:0008770

Paranoia

Occasional (5-29%)HP:0011999

physical aggression

Occasional (5-29%)HP:0000718

Related Conditions

Trimethylaminuria(parent)

Recessive hereditary disorder (autosomal)(parent)

Inborn error of metabolism(parent)

Quick Facts

SNOMED CT: 1237339005
UMLS CUI: C5575503
Fully Specified Name: Severe primary trimethylaminuria (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.