OBO ID: DOID:0111073
Term Name: progressive familial heart block Search Ontology:
  • familial Lenegre disease
  • familial Lev disease
  • familial Lev-Lenegre disease
  • familial PCCD
  • familial progressive heart block
  • hereditary bundle branch defect
  • PFHB
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. https://www.ncbi.nlm.nih.gov/pubmed/897853
Ontology: Human Disease   (DOID:0111073)
OTHER progressive familial heart block PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available