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

disorder

SNOMED 1202025005CUI C5686635

Overview

Autosomal recessive 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

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

Developmental hereditary disorder(parent)

Hereditary disorder of musculoskeletal system(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1202025005
UMLS CUI: C5686635
Fully Specified Name: Autosomal recessive 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.