All diseases

OMIM ID
605285
OMIM term:
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE
Alternative terms:
HEREDITARY MOTOR AND SENSORY NEUROPATHY, RUSSE TYPE; HMSNR
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4G; CMT4G
CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL RECESSIVE, TYPE 4G; CMT4G
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4G
(∗) Location:
10q23.2  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/bxhuent5