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progressive familial heart block

Disease Summary
Associated Targets (5)
Tbio

3

Tclin

1

Tchem

1


GARD Rare
Mondo Description Familial progressive cardiac conduction defect (PCCD) is a hereditary cardiac conduction disorder that may progress to complete atrioventricular (AV) block. The disease is either asymptomatic or manifests as dyspnea, dizziness, syncope, abdominal pain, heart failure or sudden death.
Disease Ontology Description 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 dyspnea, dizziness, syncope, abdominal pain, heart failure or sudden death.
Mondo Term and Equivalent IDs
MONDO:0019490:  progressive familial heart block
DC:0000374: 
GARD:0010005: 
OMIMPS:113900: 
Orphanet:871: 
SCTID:698249005: 
SCTID:93130009: 
UMLS:CN206278: