Autosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophy

disorder

SNOMED 771144005CUI C4749729

Overview

Autosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophy is a disorder.

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

Related Conditions

Hereditary motor and sensory neuropathy(parent)

Recessive hereditary disorder (autosomal)(parent)

Chronic nervous system disease(parent)

Quick Facts

SNOMED CT: 771144005
UMLS CUI: C4749729
Fully Specified Name: Hereditary motor and sensory neuropathy with acrodystrophy (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.