All diseases

OMIM ID
300495
OMIM term:
AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2 MENTAL RETARDATION, X-LINKED, INCLUDED
Alternative terms:

(∗) Location:
Xp22.32-p22.31  
(†) Associated OMIM genes:
NLGN4  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/37jfniz4