Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation

disorder

SNOMED 1209168005CUI C5687572

Overview

Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Congenital myopathy with fibre type disproportion(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of musculoskeletal system(parent)

Quick Facts

SNOMED CT: 1209168005
UMLS CUI: C5687572
Fully Specified Name: Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 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.