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familial long QT syndrome

Go to external page 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 ]

Synonyms: Ward-Romano syndrome familial long QT syndrome Romano-Ward long QT syndrome congenital long QT syndrome Romano-Ward syndrome hereditary long QT syndrome LQTS

This is just here as a test because I lose it

Term information

database cross reference
  • NORD:1675 (MONDO:NORD)
  • OMIMPS:192500 (MONDO:equivalentTo)
  • MedDRA:10057926 (Orphanet:768/e)
  • GARD:3284 (Orphanet:101016)
  • GARD:16547 (Orphanet:768)
  • Orphanet:768 (MONDO:equivalentTo)
  • Orphanet:101016 (OMIM:192500)
  • UMLS:C1141890 (Orphanet:768/e)
  • SCTID:442917000 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

closeMatch

http://identifiers.org/meddra/10057926

exactMatch

http://www.orpha.net/ORDO/Orphanet_101016

https://omim.org/phenotypicSeries/PS192500

http://linkedlifedata.com/resource/umls/id/C1141890

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

http://identifiers.org/snomedct/442917000

id

MONDO:0019171

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0019171

Term relations