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Echinobase
Summary Literature (0)
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


OMIM:
MIM:312750 - rett syndrome; rtt
MIM:613454 - rett syndrome, congenital variant

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): pervasive developmental disorder (is_a)