Related Conditions
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome(child)
Autosomal dominant congenital benign spinal muscular atrophy(child)
X-linked distal hereditary motor neuropathy type 3(child)
Distal hereditary motor neuropathy type 1(child)
SMARD2 - spinal muscular atrophy with respiratory distress type 2(child)
Distal hereditary motor neuropathy type 7(child)
Autosomal recessive distal spinal muscular atrophy type 4(child)
Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome(child)
Spinal muscular atrophy(parent)
Quick Facts
- SNOMED CT
- 230247001
- UMLS CUI
- C0393541
- Fully Specified Name
- Distal spinal muscular atrophy (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.