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Disease Ontology Browser
progressive familial heart block (DOID:0111073)
Alliance: disease page
Synonyms: familial Lenegre disease; familial Lev disease; familial Lev-Lenegre disease; familial PCCD; familial progressive heart block; hereditary bundle branch defect; PFHB
Alt IDs: OMIM:115080, OMIM:PS113900, ORDO:871
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.

Disease References using Mouse Models (3)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory