Autosomal recessive limb girdle muscular dystrophy type 2C

disorder

SNOMED 718176005CUI C4273683

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Autosomal recessive muscular dystrophy with limb girdle distribution(parent)

Quick Facts

SNOMED CT: 718176005
UMLS CUI: C4273683
Fully Specified Name: Autosomal recessive limb girdle muscular dystrophy type 2C (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.