RS61750240 MECP2
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What This Variant Does
"MECP2 Rett syndrome mutation
Associated Conditions
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
Encephalopathy
neonatal severeMental retardation
X-linked
syndromic 13Rett syndrome
X-linked intellectual disability-psychosis-macroorchidism syndrome
Autism
susceptibility to
X-linked 3
Syndromic X-linked intellectual disability Lubs type
Inborn genetic diseases
MECP2-related disorder
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
Other Variants in MECP2