All diseases

OMIM ID
214400
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A
Alternative terms:
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4A
(∗) Location:
8q21.11  
(†) Associated OMIM genes:
GDAP1  
(‡) Associated MGI genes:

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