All diseases

OMIM ID
312750
OMIM term:
RETT SYNDROME; RTT
Alternative terms:
RTS
AUTISM, DEMENTIA, ATAXIA, AND LOSS OF PURPOSEFUL HAND USE RETT SYNDROME, ZAPPELLA VARIANT, INCLUDED
RETT SYNDROME, PRESERVED SPEECH VARIANT, INCLUDED
RETT SYNDROME, ATYPICAL, INCLUDED
(∗) Location:
Xq28  
(†) Associated OMIM genes:
MECP2  
(‡) Associated MGI genes:
Mecp2  

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