Related Conditions
X-linked muscular dystrophy with limb girdle distribution(child)
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein(child)
Hutterite type of muscular dystrophy(child)
X-linked muscular dystrophy not predominantly limb girdle(child)
Autosomal recessive muscular dystrophy not predominantly limb girdle(child)
Autosomal dominant muscular dystrophy not predominantly limb girdle(child)
Merosin deficient congenital muscular dystrophy(child)
Muscle-eye-brain disease, congenital muscular dystrophy(child)
Salih congenital muscular dystrophy(child)
Bethlem myopathy(child)
Congenital muscular dystrophy due to lamin A/C mutation(child)
Congenital muscular hypertrophy-cerebral syndrome(child)
Western type of congenital muscular dystrophy(child)
Congenital muscular dystrophy with hyperlaxity(child)
Congenital muscular dystrophy with arthrogryposis multiplex congenita(child)
Congenita hypotonic - sclerotic muscular dystrophy(child)
Congenital muscular dystrophy with intellectual disability(child)
Congenital muscular dystrophy with integrin alpha-7 deficiency(child)
Autosomal recessive myogenic arthrogryposis multiplex congenita(child)
Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome(child)
Quick Facts
- SNOMED CT
- 111501005
- UMLS CUI
- C2937300
- Fully Specified Name
- Congenital hereditary 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.