Rett's disorder Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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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1 genes associated with the Rett's disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
MECP2 methyl CpG binding protein 2