infancy electroclinical syndrome

Summary

DOID:0050703 - infancy electroclinical syndrome

Disease Ontology Definition:An electroclinical syndrome with onset in infancy occurring between birth and one year of age.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: arx, kcnq3, ntrk2, st3gal3, stxbp1, grin2b, cdkl5, wdr45, guf1, sptan1, piga, scn8a, chrna2, phactr1, prrt2, [+]

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0000413 - infancy electroclinical syndrome

MONDO:0000413 - infancy electroclinical syndrome

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): electroclinical syndrome (is_a)