All diseases

OMIM ID
309610
OMIM term:
PRIETO X-LINKED MENTAL RETARDATION SYNDROME; PRS
Alternative terms:
MENTAL RETARDATION, X-LINKED, SYNDROMIC 2; MRXS2
MENTAL RETARDATION, X-LINKED, WITH DYSMORPHISM AND CEREBRAL ATROPHY
(∗) Location:
Xp11-q21  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/1wouiaqc