| Dataset | CTD Gene-Disease Associations |
| 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) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D015518 |
| Similar Terms | |
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3 genes/proteins associated with the disease Rett Syndrome from the curated CTD Gene-Disease Associations dataset.
