DOID:0111073 - progressive familial heart block
Disease Ontology Definition:A heart conduction disease characterized by autosomal dominant inheritance of a cardiac conduction defect that may progress to complete atrioventricular (AV) block and maybe asymptomatic of manifest as shortness of breath, dizziness, syncope, abdominal pain, heart failure or sudden death.
Synonyms: PFHB, familial Lenegre disease, familial Lev disease, familial Lev-Lenegre disease, familial PCCD, familial progressive heart block, hereditary bundle branch defect,
Xenbase Genes : trpm4, scn1b, scn5a
|MONDO:0019490 - progressive familial heart block|
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): heart conduction disease (is_a)