All diseases

OMIM ID
607791
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D; CMTDID
Alternative terms:
CHARCOT-MARIE-TOOTH NEUROPATHY, DOMINANT INTERMEDIATE D
DI-CMTD
(∗) Location:
1q23.3  
(†) Associated OMIM genes:
MPZ  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ag8ifz4g