All diseases

OMIM ID
601455
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D
Alternative terms:
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE 4D
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D
HMSN4D
(∗) Location:
8q24.22  
(†) Associated OMIM genes:
NDRG1  
(‡) Associated MGI genes:
Ndrg1  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/dy3qtj08