All diseases

OMIM ID
605589
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2; CMT2B2
Alternative terms:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE B2
CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2B2
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2B2
ARCMT2B
(∗) Location:
19q13.33  
(†) Associated OMIM genes:
MED25  
(‡) Associated MGI genes:

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