All diseases

OMIM ID
607736
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J; CMT2J
Alternative terms:
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2J
CHARCOT-MARIE-TOOTH DISEASE, TYPE 2, WITH HEARING LOSS AND PUPILLARY ABNORMALITIES
(∗) Location:
1q23.3  
(†) Associated OMIM genes:
MPZ  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/1pce9tgu