rett syndrome Gene Set

Dataset OMIM Gene-Disease 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)
External Link http://www.omim.org/entry/312750
Similar Terms
Downloads & Tools

Genes

1 genes associated with the rett syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
MECP2 methyl CpG binding protein 2