All diseases

OMIM ID
145900
OMIM term:
HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS
Alternative terms:
DEJERINE-SOTTAS SYNDROME; DSS
CHARCOT-MARIE-TOOTH DISEASE, TYPE 3; CMT3
HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE III; HMSN3
DEJERINE-SOTTAS NEUROPATHY; DSN
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F
(∗) Location:
10q21.3   17p12   19q13.2   1q23.3  
(†) Associated OMIM genes:
EGR2   MPZ   PMP22   PRX  
(‡) Associated MGI genes:
Mpz  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/rzm3a12s