Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N mutation

disorder

SNOMED 1202024009CUI C5686634

Overview

Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N 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 SELENON mutation(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of musculoskeletal system(parent)

Quick Facts

SNOMED CT: 1202024009
UMLS CUI: C5686634
Fully Specified Name: Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N 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.