symbol withdrawn CMT2D

Preferred Label : symbol withdrawn CMT2D;

Obsolete resource : true;

Approved symbol HGNC : CMT2D;

Chromosome HGNC : 7p14;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:14684;

Automatic exact mappings (from CISMeF team)
- Charcot-marie-tooth disease, axonal, type 2d [OMIM Phenotype]
Replaced by
- glycyl-tRNA synthetase 1 [HGNC gene]

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