Overview
Hereditary progressive muscular dystrophy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Distal muscular dystrophy(child)
Muscular dystrophy with predominantly proximal limb girdle distribution(child)
Congenital hereditary muscular dystrophy(child)
X-linked scapuloperoneal muscular dystrophy(child)
SCARMD - Severe childhood autosomal recessive muscular dystrophy(child)
EDMD2 - autosomal dominant Emery-Dreifuss muscular dystrophy(child)
Autosomal recessive Emery-Dreifuss muscular dystrophy(child)
X-linked Emery-Dreifuss muscular dystrophy(child)
X-linked myopathy with postural muscle atrophy(child)
DM - dystrophia myotonica(child)
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome(child)
Muscular dystrophy(parent)
Hereditary disorder of musculoskeletal system(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 193225000
- UMLS CUI
- C4551827
- Fully Specified Name
- Hereditary progressive muscular dystrophy (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.