All diseases

OMIM ID
608673
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L
Alternative terms:
CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, TYPE 2L
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2L
(∗) Location:
12q24.23  
(†) Associated OMIM genes:
HSPB8  
(‡) 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/hy1s9fkc