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long QT syndrome

^ http://purl.obolibrary.org/obo/MONDO_0002442

A condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward syndrome (also known as long QT syndrome 1) and Jervell-Lange Nielsen syndrome. [ MESH:D008133 ]

Term info

database cross reference
  • ICD9:426.82 (DOID:2843)
  • NCIT:C34786 (MONDO:equivalentTo)
  • MESH:D008133 (MONDO:equivalentTo)
  • ICD10CM:I45.81 (MONDO:equivalentTo)
  • UMLS:C0023976 (NCIT:C34786)
  • DOID:2843 (MONDO:equivalentTo)
abbreviation
LQT [ DOID:2843 ]

definition

A condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward syndrome (also known as long QT syndrome 1) and Jervell-Lange Nielsen syndrome.

exactMatch

http://purl.obolibrary.org/obo/DOID_2843, http://purl.bioontology.org/ontology/ICD10CM/I45.81, http://identifiers.org/mesh/D008133, http://purl.obolibrary.org/obo/NCIT_C34786, http://linkedlifedata.com/resource/umls/id/C0023976

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0000591

has exact synonym

ventricular arrhythmia associated with long QT syndrome, long QT syndrome, LQT, long Q-T syndrome

id

MONDO:0002442