All diseases

OMIM ID
300243
OMIM term:
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE; MRXSCH
Alternative terms:
ANGELMAN-LIKE SYNDROME, X-LINKED
MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND ATAXIA SYNDROME
(∗) Location:
Xq26.3  
(†) Associated OMIM genes:
SLC9A6  
(‡) Associated MGI genes:

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