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familial long QT syndrome

^ http://purl.obolibrary.org/obo/MONDO_0019171

A hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias. [ Orphanet:768 ]

Term info

database cross reference
  • UMLS:C0035828 (Orphanet:101016/e)
  • OMIMPS:192500 (MONDO:equivalentTo)
  • UMLS:C1141890 (Orphanet:768/e)
  • SCTID:442917000 (MONDO:equivalentTo)
  • Orphanet:101016 (OMIM:192500)
  • Orphanet:768 (MONDO:equivalentTo)
  • MedDRA:10057926 (Orphanet:768/e)
Subsets

ordo_disease, clingen

abbreviation
LQTS [ Orphanet:768 ]

closeMatch

http://identifiers.org/meddra/10057926

definition

A hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias.

exactMatch

https://omim.org/phenotypicSeries/PS192500, http://linkedlifedata.com/resource/umls/id/C1141890, http://linkedlifedata.com/resource/umls/id/C0035828, http://purl.obolibrary.org/obo/Orphanet_101016, http://identifiers.org/snomedct/442917000, http://purl.obolibrary.org/obo/Orphanet_768

has exact synonym

Ward-Romano syndrome, familial long QT syndrome, Romano-Ward long QT syndrome, Romano-Ward syndrome, hereditary long QT syndrome, congenital long QT syndrome, LQTS

id

MONDO:0019171

Term relations