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Familial long QT syndrome

^ http://www.orpha.net/ORDO/Orphanet_768


Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias.

Synonyms: Congenital long QT syndrome

Term info

database cross reference
  • OMIM:613693 (BTNT (broader term maps to a narrower term))
  • OMIM:611818 (BTNT (broader term maps to a narrower term))
  • MedDRA:10057926 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:612347 (BTNT (broader term maps to a narrower term))
  • OMIM:603830 (BTNT (broader term maps to a narrower term))
  • OMIM:611820 (BTNT (broader term maps to a narrower term))
  • ICD-10:I45.8 (Attributed)
  • OMIM:601005 (BTNT (broader term maps to a narrower term))
  • OMIM:611819 (BTNT (broader term maps to a narrower term))
  • OMIM:612955 (BTNT (broader term maps to a narrower term))
  • UMLS:C1141890 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:192500 (BTNT (broader term maps to a narrower term))
  • OMIM:220400 (BTNT (broader term maps to a narrower term))
  • ICD-10:I45.8 (NTBT (narrower term maps to a broader term))
  • OMIM:616249 (BTNT (broader term maps to a narrower term))
  • OMIM:616247 (BTNT (broader term maps to a narrower term))
  • OMIM:613485 (BTNT (broader term maps to a narrower term))
  • OMIM:613688 (BTNT (broader term maps to a narrower term))
  • OMIM:600919 (BTNT (broader term maps to a narrower term))
  • OMIM:613695 (BTNT (broader term maps to a narrower term))
hasDbXref

OMIM:611818, OMIM:611819, OMIM:601005, MedDRA:10057926, OMIM:220400, OMIM:603830, OMIM:192500, OMIM:613485, OMIM:613693, OMIM:616247, OMIM:600919, OMIM:613695, OMIM:612347, OMIM:613688, OMIM:616249, OMIM:611820, OMIM:612955, ICD-10:I45.8, UMLS:C1141890

notation

ORPHA:768