All diseases

OMIM ID
300238
OMIM term:
MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11
Alternative terms:
SHASHI X-LINKED MENTAL RETARDATION SYNDROME; SMRXS
MENTAL RETARDATION, X-LINKED, SHASHI TYPE
(∗) Location:
Xq26-q27  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/u34v598t