Familial methionine malabsorption

disorder

SNOMED 45812003CUI C0268622

Overview

Familial methionine malabsorption is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Aminoaciduria

HP:0003355

Blue irides

HP:0000635

Diarrhea

HP:0002014

Epilepsy

HP:0001250

Mental-retardation

HP:0001249

Positive FeCl3 test

HP:0003612

Tachypnea

HP:0002789

White hair

HP:0011364

Related Conditions

Specific renal tubule transport defect(parent)

Disorder of sulphur-bearing amino acid metabolism(parent)

Metabolic renal disease(parent)

Quick Facts

SNOMED CT: 45812003
UMLS CUI: C0268622
Fully Specified Name: Familial methionine malabsorption (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.