childhood electroclinical syndrome

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

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 - childhood electroclinical syndrome

MONDO:0000414 - childhood 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)