| Disease Aliases (30) | Autism, dementia, ataxia, and loss of purposeful hand use Autism dementia ataxia loss of purposeful hand use syndrome Autism-dementia-ataxia-loss of purposeful hand use syndrome Cerebroatrophic hyperammonemia Cerebroatrophic hyperammonemias Cerebroatrophic hyperammonaemia Classic rett syndrome Hyperammonemia, cerebroatrophic Hyperammonemias, cerebroatrophic Mecp2-related disorders Mrxs13 Ppmx Rett dis Rett syndrome, atypical Rett syndrome, preserved speech variant Rett syndrome, zappella variant Retts dis Rts Rts - rett syndrome Rtt Rett disorder Rett syndrome; rtt Rett's disorder Rett's syndrome Rett's disorder (disorder) Retts syndrome Syndrome, rett Syndrome, rett's X-linked mental retardation, syndromic 13 |
Associated Genes (1) NCBI-RefSeq: MECP2 (Methyl-CpG binding protein 2) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Rett syndrome | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |