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DOID:0110653 - long QT syndrome 12
Disease Ontology Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21.
Synonyms: LQT12,
Echinobase Genes :
MIM:612955 - long qt syndrome 12; lqt12 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
long QT syndrome (is_a)