charcot-marie-tooth disease

Preferred Label : charcot-marie-tooth disease;

MedlinePlus synonym : peroneal muscular atrophy; hereditary motor and sensory neuropathy;

Details

Origin ID

T1260;

UMLS CUI

C0007959;

Automatic exact mappings (from CISMeF team)
- Charcot-Marie-Tooth disease type 1B [DO Concept]
- Charcot-Marie-Tooth disease type 4 [DO Concept]
- Charcot-marie-tooth disease, demyelinating, type 1b [OMIM Phenotype]
- motor peripheral neuropathy [DO Concept]
Currated CISMeF NLP mapping
- Charcot Marie Tooth disease [PASCAL descriptor]
- Charcot Marie Tooth disease [Disease (Nov.)]
- Charcot-Marie-Tooth Disease [NCIt concept]
- Charcot-Marie-Tooth disease [Radlex concept]
- Charcot-Marie-Tooth disease [DO Concept]
- Charcot-Marie-Tooth disease [MeSH concept]
- Charcot-Marie-Tooth disease [MedDRA LLT]
- Charcot-Marie-Tooth disease (disorder) [Inactive SNOMED CT concept]
- Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy [ORDO Disease]
- Charcot-marie-tooth disease [OMIM phenotypic series]
- Hereditary motor and sensory neuropathy [ICD-10 Sub-category]
- Hereditary motor and sensory neuropathy [ICD-10 Sub-category (who)]
- Hereditary motor and sensory neuropathy [ORDO Disease]
- Hereditary motor and sensory neuropathy [ICD-11 Category]
- Hereditary motor and sensory neuropathy [MedDRA Preferred Term]
- Hereditary motor and sensory neuropathy (disorder) [SNOMED CT concept]
- Hereditary sensory and autonomic neuropathy [ORDO Disease]
- Hereditary sensory and autonomic neuropathy (disorder) [SNOMED CT concept]
- Hereditary sensory or autonomic neuropathy [ICD-11 Category]
- Peroneal muscular atrophy [MedDRA LLT]
- Peroneal muscular atrophy [ICD-9 code]
- charcot-marie-tooth disease [MeSH Descriptor]
- hereditary motor sensory neuropathy [Disease (Nov.)]
- hereditary sensory and autonomic neuropathies [MeSH Descriptor]
- hereditary sensory and autonomic neuropathies [MeSH concept]
- hereditary sensory and motor neuropathy [MeSH Descriptor]
- hereditary sensory and motor neuropathy [MeSH concept]
- peroneal muscular atrophy [SNOMED Notion]
MeSH descriptor(s)
- charcot-marie-tooth disease [MeSH Descriptor]
See also
- degenerative nerve diseases [MedlinePlus Topic]
- muscle disorders [MedlinePlus Topic]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Charcot Marie Tooth disease [PASCAL descriptor]
- Charcot Marie Tooth disease [Disease (Nov.)]
- Charcot-Marie-Tooth Disease [NCIt concept]
- Charcot-Marie-Tooth disease [MeSH concept]
- Charcot-Marie-Tooth disease [DO Concept]
- Charcot-Marie-Tooth disease [MedDRA LLT]
- Charcot-Marie-Tooth disease (disorder) [Inactive SNOMED CT concept]
- Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy [ORDO Disease]
- Peroneal muscular atrophy [MedDRA Preferred Term]
- Peroneal muscular atrophy [ICD-9 code]
- Peroneal muscular atrophy [MedDRA LLT]
- charcot-marie-tooth disease [MeSH Descriptor]
- peroneal muscular atrophy [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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