Charcot-Marie-Tooth disease, demyelinating, type 1e

Preferred Label : Charcot-Marie-Tooth disease, demyelinating, type 1e;

MeSH synonym : Charcot-Marie-Tooth neuropathy and deafness, autosomal dominant; Cmt1e;

Details

Origin ID

C566136;

UMLS CUI

C3495591;

Automatic exact mappings (from CISMeF team)
- PMP22 wt Allele [NCIt concept]
Currated CISMeF NLP mapping
- Charcot-Marie-Tooth disease type 1E [DO Concept]
- Charcot-Marie-Tooth disease type 1E [ORDO Disease]
- Charcot-marie-tooth disease and deafness [OMIM Phenotype]
MeSH term(s) associated for indexing
- charcot-marie-tooth disease [MeSH Descriptor]
- deafness [MeSH Descriptor]
Record concept(s)
- Charcot-Marie-Tooth disease, demyelinating, type 1e [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Charcot-marie-tooth disease and deafness [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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