rett syndrome Gene Set

Dataset	DISEASES Curated Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A pervasive developmental disease that is a neurological and developmental disorder that mostly occurs in females and is caused_by a mutation on the MECP2 gene on the X chromosome. Infants with Rett syndrome seem to grow and develop normally at first, but then stop developing and even lose skills and abilities. (Human Disease Ontology, DOID_1206)
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Genes

1 genes involed in the disease rett syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name
MECP2	methyl CpG binding protein 2