All diseases

OMIM ID
300486
OMIM term:
MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE
Alternative terms:

(∗) Location:
Xq12  
(†) Associated OMIM genes:
OPHN1  
(‡) Associated MGI genes:
Ophn1  

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* quick link - http://q.sanger.ac.uk/w98ntlt8