Charcot-Marie-Tooth disease, X-linked, 1

Preferred Label : Charcot-Marie-Tooth disease, X-linked, 1;

MeSH synonym : hereditary motor and sensory neuropathy, X-linked; HMSN, X-linked; Charcot-Marie-Tooth peroneal muscular atrophy, X-linked; CMTX 1; Charcot-Marie-Tooth neuropathy, X-Linked, 1; Cmtx1;

Details

Origin ID

C535919;

UMLS CUI

C0393808;

Currated CISMeF NLP mapping
- Charcot-Marie-Tooth Neuropathy X Type 1 [NCIt concept]
- Charcot-Marie-Tooth disease X-linked dominant 1 [DO Concept]
- Charcot-marie-tooth disease, X-linked dominant, 1 [OMIM Phenotype]
- X-linked Charcot-Marie-Tooth disease type 1 [ORDO Disease]
- X-linked Charcot-Marie-Tooth disease type 1 (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- charcot-marie-tooth disease [MeSH Descriptor]
ORDO relation(s)
- X-linked Charcot-Marie-Tooth disease type 1 [ORDO Disease]
Record concept(s)
- Charcot-Marie-Tooth disease, X-linked, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Charcot-Marie-Tooth Neuropathy X Type 1 [NCIt concept]
- Charcot-Marie-Tooth disease X-linked dominant 1 [DO Concept]
- Charcot-marie-tooth disease, X-linked dominant, 1 [OMIM Phenotype]
- X-linked Charcot-Marie-Tooth disease type 1 [ORDO Disease]
- X-linked Charcot-Marie-Tooth disease type 1 (disorder) [SNOMED CT concept]
Validated automatic mappings to NTBT
- X-linked Charcot-Marie-Tooth disease [ORDO Disease]

Keyword's position in hierarchy(ies) :

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