Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)

Preferred Label : Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive);

Obsolete resource : true;

Approved symbol HGNC : CMTX2;

Chromosome HGNC : Xp22;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:2137;

UMLS CUI

C1413539;

Automatic exact mappings (from CISMeF team)
- Charcot-marie-tooth disease, X-linked recessive, 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CMTX2 gene [LOINC component]

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