MME-related autosomal dominant Charcot Marie Tooth disease type 2

disorder

SNOMED 1172585006CUI C5567450

Overview

MME-related autosomal dominant Charcot Marie Tooth disease type 2 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)

Chronic nervous system disease(parent)

Peripheral nerve disease(parent)

Quick Facts

SNOMED CT: 1172585006
UMLS CUI: C5567450
Fully Specified Name: Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease 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.