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Autosomal dominant muscular dystrophy with limb girdle distribution

disorder
SNOMED 240067001CUI C0410184

Overview

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

Related Conditions

Autosomal dominant muscular dystrophy with gene located at 5q31(child)
Autosomal dominant limb girdle muscular dystrophy type 1D(child)
Autosomal dominant limb girdle muscular dystrophy type 1E(child)
Autosomal dominant limb girdle muscular dystrophy type 1F(child)
Autosomal dominant limb girdle muscular dystrophy type 1G(child)
Autosomal dominant limb-girdle muscular dystrophy type 1H(child)
Calpain-3-related limb girdle muscular dystrophy D4(child)
Muscular dystrophy with predominantly proximal limb girdle distribution(parent)
Autosomal dominant hereditary disorder(parent)

Quick Facts

SNOMED CT
240067001
UMLS CUI
C0410184
Fully Specified Name
Autosomal dominant muscular dystrophy with limb girdle distribution (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.