All diseases

OMIM ID
601472
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D
Alternative terms:
CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2D
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2D
(∗) Location:
7p14.3  
(†) Associated OMIM genes:
GARS  
(‡) Associated MGI genes:
Gars  

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