← Back to Conditions
Autosomal recessive demyelinating Charcot-Marie-Tooth
disorderSNOMED 715795005CUI C4082197
Overview
Autosomal recessive demyelinating Charcot-Marie-Tooth is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Charcot-Marie-Tooth disease type 4A(child)
Charcot-Marie-Tooth disease type 4C(child)
Charcot-Marie-Tooth disease type 4D(child)
Charcot-Marie-Tooth disease type 4G(child)
Charcot-Marie-Tooth disease type 4B2(child)
Charcot-Marie-Tooth disease type 4F(child)
Charcot-Marie-Tooth disease type 4H(child)
Charcot-Marie-Tooth disease type 4B1(child)
Charcot-Marie-Tooth disease type 4J(child)
Charcot-Marie-Tooth disease type 4E(child)
Charcot-Marie-Tooth disease type 4B3(child)
Charcot-Marie-Tooth disease type 4K(child)
Recessive hereditary disorder (autosomal)(parent)
Hereditary motor and sensory neuropathy(parent)
Congenital disease(parent)
Quick Facts
- SNOMED CT
- 715795005
- UMLS CUI
- C4082197
- Fully Specified Name
- Charcot-Marie-Tooth disease type 4 (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.