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

This is just here as a test because I lose it

Term information

database cross reference
  • 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)
Subsets

gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare

exactMatch

http://purl.obolibrary.org/obo/DOID_0111073

http://www.orpha.net/ORDO/Orphanet_871

http://identifiers.org/snomedct/698249005

https://omim.org/phenotypicSeries/PS113900

has narrow synonym

hereditary bundle branch defect

has related synonym

familial progressive cardiac conduction defect

id

MONDO:0019490

Term relations