Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation

disorder

SNOMED 1208417009CUI C5687105

Overview

Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation is a disorder.

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

Related Conditions

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

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1208417009
UMLS CUI: C5687105
Fully Specified Name: Autosomal recessive 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.

Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation — Symptoms, Testing & Specialists | Ltrl | Healos