Autosomal dominant congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation

disorder

SNOMED 1208418004CUI C5687106

Overview

Autosomal dominant congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation(parent)

Quick Facts

SNOMED CT: 1208418004
UMLS CUI: C5687106
Fully Specified Name: Autosomal dominant congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.