All diseases

OMIM ID
309510
OMIM term:
PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS
Alternative terms:
PARTINGTON SYNDROME
MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1
MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, AND SEIZURES
MENTAL RETARDATION, X-LINKED 36; MRX36
(∗) Location:
Xp21.3  
(†) Associated OMIM genes:
ARX  
(‡) Associated MGI genes:

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