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. [ Orphanet:871 ]
Synonyms: familial progressive heart block familial Lev-Lenègre disease PFHB familial Lenegre disease familial Lev disease familial Lenègre disease familial PCCD familial Lev-Lenegre disease
Term information
- SCTID:93130009 (MONDO:equivalentObsolete)
- SCTID:698249005 (MONDO:equivalentTo)
- Orphanet:871 (MONDO:equivalentTo)
- OMIMPS:113900 (MONDO:equivalentTo)
- GARD:10005 (MONDO:GARD)
- ICD9:426.6 (MONDO:relatedTo)
- DOID:0111073 (MONDO:equivalentTo)
gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare
http://purl.obolibrary.org/obo/DOID_0111073
http://www.orpha.net/ORDO/Orphanet_871
http://identifiers.org/snomedct/698249005
https://omim.org/phenotypicSeries/PS113900