A rare group of genetic, cardiac rhythm diseases characterized by a prolongation of the QT interval at basal electrocardiography (ECG) and by a high risk of life-threatening arrhythmias.

Synonyms:

LQTS

Congenital long QT syndrome

This is just here as a test because I lose it

Term information

database cross reference
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=768
hasDbXref
  • OMIM:611818
  • OMIM:611819
  • OMIM:601005
  • MedDRA:10057926
  • OMIM:220400
  • OMIM:603830
  • OMIM:192500
  • OMIM:613485
  • OMIM:600919
  • OMIM:613693
  • OMIM:616247
  • OMIM:613695
  • OMIM:612347
  • OMIM:618447
  • OMIM:616249
  • OMIM:613688
  • OMIM:611820
  • ICD-10:I45.8
  • OMIM:612955
  • UMLS:C1141890
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409948
  • http://www.orpha.net/ORDO/Orphanet_409947
  • http://www.orpha.net/ORDO/Orphanet_409946
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409929
  • http://www.orpha.net/ORDO/Orphanet_409930
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409981
notation
  • ORPHA:768
  • Clinical group
present in
  • http://www.orpha.net/ORDO/Orphanet_409991

Term relations