All diseases

OMIM ID
301835
OMIM term:
ARTS SYNDROME; ARTS
Alternative terms:
MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS
ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION
MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18
(∗) Location:
Xq22.3  
(†) Associated OMIM genes:
PRPS1  
(‡) Associated MGI genes:

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