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DOID:0110644 - long QT syndrome 1
Disease Ontology Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.
Synonyms: LQT1, ventricular fibrillation with prolonged QT interval,
Echinobase Genes :
MIM:192500 - long qt syndrome 1; lqt1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
long QT syndrome (is_a)