All diseases

OMIM ID
118300
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS
Alternative terms:
CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E
(∗) Location:
17p12  
(†) Associated OMIM genes:
PMP22  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/ddrk5z95