All diseases

OMIM ID
607734
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F
Alternative terms:

(∗) Location:
8p21.2  
(†) Associated OMIM genes:
NEFL  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/1vzzpe2f