Autosomal dominant distal spinal muscular atrophy type 2

disorder

SNOMED 1230343006CUI C5575565

Overview

Autosomal dominant distal spinal muscular atrophy type 2 is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Autosomal dominant distal hereditary motor neuropathy(parent)

Chronic nervous system disease(parent)

Quick Facts

SNOMED CT: 1230343006
UMLS CUI: C5575565
Fully Specified Name: Distal hereditary motor neuropathy type 2 (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.