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Autosomal recessive Charcot-Marie-Tooth disease type 2

disorder
SNOMED 1156852009CUI C5548216

Overview

Autosomal recessive Charcot-Marie-Tooth disease type 2 is a disorder.

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

Related Conditions

Autosomal recessive axonal Charcot-Marie-Tooth disease type 2T(child)
Severe early-onset axonal neuropathy due to NEFL (neurofilament light) deficiency(child)
Charcot-Marie-Tooth disease type 2R(child)
Charcot-Marie-Tooth disease type 2B2(child)
Charcot-Marie-Tooth disease type 2H(child)
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness(child)
Charcot-Marie-Tooth disease type 2B1(child)
Autosomal recessive Charcot-Marie-Tooth disease type 2X(child)
Charcot-Marie-Tooth disease type 2S(child)
DNAJB2-related Charcot-Marie-Tooth disease type 2(child)
Recessive hereditary disorder (autosomal)(parent)
Charcot-Marie-Tooth disease, type II(parent)

Quick Facts

SNOMED CT
1156852009
UMLS CUI
C5548216
Fully Specified Name
Autosomal recessive 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.