Dejerine-Sottas syndrome

Preferred Label : Dejerine-Sottas syndrome;

ICD-11 synonym : Déjerine-Sottas neuropathy; hypertrophic demyelinative neuropathy of infancy; Dejerine-Sottas disease; HSMN 3 - [hereditary motor and sensory neuropathy type 3]; HMSN3 - [Hereditary motor and sensory neuropathy type 3]; Charcot-Marie-Tooth disease type 3; Déjerine-Sottas neuritis; CMT3 - [Charcot-Marie-Tooth disease type 3]; Hereditary motor or sensory neuropathy type 3; Hypertrophic neuropathy of infancy; hereditary motor and sensory neuropathy type 3;

ICD-11 acronym : CMT3; HMSN3; HSMN 3;

ICD-11 inclusion : Hypertrophic neuropathy of infancy;

Details

Origin ID

418660830;

Automatic exact mappings (from CISMeF team)
- CMT-3 [MeSH concept]
- Hereditary motor and sensory neuropathy [ICD-10 Sub-category]
- hereditary sensory and motor neuropathy [MeSH Descriptor]
- tetracycline CMT-3 [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Charcot-Marie-Tooth disease type 3 [DO Concept]
- Dejerine-Sottas Neuropathy [NCIt concept]
- Dejerine-Sottas neuropathy [PASCAL descriptor]
- Dejerine-Sottas syndrome [ORDO Disease]
- Déjérine-Sottas disease (disorder) [SNOMED CT concept]
- HMSN type III [MeSH concept]
- Hypertrophic neuropathy of dejerine-sottas [OMIM Phenotype]
- dejerine-sottas disease [SNOMED Notion]
- hereditary motor and sensory polyneuropathy type III [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients