symbol withdrawn CMT2B

Preferred Label : symbol withdrawn CMT2B;

Obsolete resource : true;

Approved symbol HGNC : CMT2B;

Chromosome HGNC : 3q13-q22;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:2132;

UMLS CUI

C1413536;

Automatic exact mappings (from CISMeF team)
- Charcot-marie-tooth disease, axonal, type 2b [OMIM Phenotype]
Replaced by
- RAB7A, member RAS oncogene family [HGNC gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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