All diseases

OMIM ID
300423
OMIM term:
MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH
Alternative terms:

(∗) Location:
Xp11.4  
(†) Associated OMIM genes:
ATP6AP2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/t6irjxd3