All diseases

OMIM ID
606595
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F
Alternative terms:
CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2F
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2F
(∗) Location:
7q11.23  
(†) Associated OMIM genes:
HSPB1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/2jm20fz2