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DOID:1206 - Rett syndrome
Disease Ontology Definition:A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability.
Synonyms: Rett's disorder, cerebroatrophic hyperammonemia,
Echinobase Genes
:
foxg1
| MIM:312750 - rett syndrome; rtt |
| MIM:613454 - rett syndrome, congenital variant |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
pervasive developmental disorder (is_a)