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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: familial Lenegre disease, familial Lev disease, familial Lev-Lenegre disease, familial PCCD, familial progressive heart block, hereditary bundle branch defect, PFHB
Xenbase Genes
:
trpm4,
scn1b,
akap10,
scn5a
| MONDO:0019490 - progressive familial heart block |
| MIM:115080 - CARDIAC CONDUCTION DEFECT |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
heart conduction disease (is_a)