childhood electroclinical syndrome

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Summary

Literature (0)

DOID:0050704 - childhood electroclinical syndrome

Disease Ontology Definition:An electroclinical syndrome with onset in childhood between one and 12 years 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

: cux2, chd2, scn1a, dnm1, grin2a, mapk10, slc2a1, gabrg2, gabrb3, cacna1h

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0000414 - mucous gland

MONDO:0000414 - mucous gland

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

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

Parent(s): absence epilepsy (is_a), electroclinical syndrome (is_a)