Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation

disorder

SNOMED 764730007CUI C4707173

Overview

Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation is a disorder.

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

Related Conditions

Autosomal dominant Charcot-Marie-Tooth disease type 2(parent)

Quick Facts

SNOMED CT: 764730007
UMLS CUI: C4707173
Fully Specified Name: Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation (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.