OBO ID: DOID:0111073
Term Name: progressive familial heart block Search Ontology:
Synonyms:
  • 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
References:
Ontology: Human Disease   ( DOID:0111073 )
Relationships
is a type of:
has subtype:
OTHER progressive familial heart block PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.