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long QT syndrome

Go to external page 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 ]

Synonyms: ventricular arrhythmia associated with long QT syndrome long QT syndrome LQT long Q-T syndrome

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Term information

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

clingen

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

id

MONDO:0002442

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0002442

Term relations