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#312750 - RETT SYNDROME; RTT
RETT SYNDROME, ZAPPELLA VARIANT, INCLUDED
Cytogenetic locations: Xq26.1
Gene summaries Genetic tests Medical literature
#300673 - ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
#300496 - AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3
#300260 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL
#300055 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 13; MRXS13
*300005 - METHYL-CpG-BINDING PROTEIN 2; MECP2
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