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DOID:0080468 - developmental and epileptic encephalopathy 1
Disease Ontology Definition:A developmental and epileptic encephalopathy characterized by X-linked recessive inheritance of frequent tonic seizures or spasms beginning in infancy that has_material_basis_in mutation in the ARX gene on chromosome Xp21.
Synonyms: DEE1, X-linked infantile spasm syndrome 1, early infantile epileptic encephalopathy 1,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee