All diseases

OMIM ID
309555
OMIM term:
MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES
Alternative terms:

(∗) Location:
Xq26  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/xeb9wm28