SHMARQL

Jervell-Lange Nielsen syndrome

<http://www.wikidata.org/entity/Q3304152>

Human disease
rdfs:label
"Jervell-Lange Nielsen syndrome"@en
skos:altLabel
"Cardioauditory syndrome of Jervell and Lange-Nielsen"@en
"Deafness, congenital, and functional heart disease"@en
"JLNS1"@en
"Jervell Lange-Nielsen syndrome"@en
"Jervell and Lange-Nielsen syndrome"@en
"Jervell and Lange-Nielson syndrome"@en
"Jervell and Lange-Nielson syndrome (disorder)"@en
"Jervell and Lange-Nielson syndrome (finding)"@en
"Prolonged QT interval in EKG and sudden death"@en
"Surdo-cardiac syndrome"@en
"long QT Jervell and Lange-Nielsen syndrome"@en
schema:description
"Human disease"@en
schema:dateModified "2026-10-24T00:42:03+00:00"^^xsd:dateTime
schema:version 2560168107
wikibase:identifiers 19
21
wikibase:sitelinks 8
wikibase:statements 47
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p:P1343 wd:statement/Q3304152-73bf14a1-43e7-a069-60d4-ed9084d0ff53
p:P138 wd:statement/Q3304152-0c0a92ac-4a9c-e81c-9940-f5abe46ff7c9
wd:statement/Q3304152-1d2f7484-4f38-4797-655d-7d889044a11c
p:P14914 wd:statement/Q3304152-BF57FBE0-368F-40BE-9D89-286DF2A65598
p:P1550 wd:statement/Q3304152-5205B8E2-BB04-468D-B289-B2029F6E1488
p:P1748 wd:statement/Q3304152-86172760-0765-444B-9D22-0E0043C38794
p:P1995 wd:statement/Q3304152-79D2B27F-A9A1-4454-9C16-356D8A17226D
p:P2293 wd:statement/Q3304152-06CDD6F5-759A-4706-A494-251D2369EEB5
wd:statement/Q3304152-134AE112-8EFE-44E5-AF1E-056360271153
p:P279 wd:statement/Q3304152-7B285701-A8E6-4DBF-BD2D-23FB0F44CD8A
p:P2841 wd:statement/Q3304152-571D3F46-7AE2-452C-BB73-B82C0FD0C3FC
p:P2888 wd:statement/Q3304152-078BD925-8688-41C8-B91B-F007EFE46781
wd:statement/Q3304152-823C5FAE-C185-490C-BDBE-27E64836CADC
wd:statement/Q3304152-AB40F5EE-ECFC-413D-87D3-130FF1755C9B
p:P2892 wd:statement/Q3304152-1EC2D257-1ED2-4F0C-B85B-049D2451B93B
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wd:statement/Q3304152-F51AC460-634F-488D-AA99-7F40DDF0D535
p:P4317 wd:statement/Q3304152-AF7100B0-B1FA-48DE-9BE0-191EFDFE22D8
p:P486 wd:statement/Q3304152-5C53F8AF-42FE-437C-9985-7224A1D5776D
p:P492 wd:statement/Q3304152-47F6EC05-1A33-48D1-941C-E697D7389A7E
wd:statement/Q3304152-FBEB42CA-A265-410F-BE63-52A159368CEB
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p:P5008 wd:statement/Q3304152-8FD9BDC9-73A9-4B94-8AB0-1EBBD69E6C6E
p:P5270 wd:statement/Q3304152-F37CA117-1DCA-429D-AF06-B5620427AB4E
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p:P6366 wd:statement/Q3304152-0F4DA0F4-F02E-4446-99E5-9D82D0BF8BA9
p:P646 wd:statement/Q3304152-AF8315DC-A550-4801-B41F-094A4AC58433
p:P6532 wd:statement/Q3304152-052ADB40-04CA-44D6-B6AC-27A888D9F082
wd:statement/Q3304152-3603827D-3499-43E5-A0E2-48D0189E044F
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wd:statement/Q3304152-67A01122-A248-4723-B3D6-4CADC62511EB
wd:statement/Q3304152-7E8F1A29-37F4-4DB5-8A2C-4F038D3D4DC6
wd:statement/Q3304152-7EEEC8B1-3C5A-4851-81E9-C7B08784A9C9
wd:statement/Q3304152-9E11103B-6FCC-4364-9D37-89890515D904
wd:statement/Q3304152-AA03EFDB-5959-4FFC-844C-D13816724FA6
wd:statement/Q3304152-BA962D25-2EE3-4505-BA56-CBCB916F6941
wd:statement/Q3304152-CFE60C8E-66B0-4CCC-A9F1-C23A0C04BFE0
wd:statement/Q3304152-DED369B2-9A0D-4859-A9D1-814A69506F48
p:P665 wd:statement/Q3304152-5E389AB3-D111-4525-9A56-752B1AD4554E
p:P668 wd:statement/q3304152-B99465F1-BCA2-49F1-8A49-03F0340B94AC
p:P672 wd:statement/Q3304152-0E50D674-7639-49CA-97D8-901A018F2590
wd:statement/Q3304152-12B54451-1AE3-49D0-8C0B-10458E70E155
wd:statement/Q3304152-5dcf6983-4217-367e-68b6-122e09348a41
p:P699 wd:statement/Q3304152-C2951204-42CC-4D1A-9325-560645C6B777
p:P7464 wd:statement/Q3304152-9D8DDBC2-8CA2-459E-84D7-99047DA17D69
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D029593>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0002441>
p:direct-normalized/P6366 <https://makg.org/entity/2778026839>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H02091>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C14.280.067.565.440>
<http://id.nlm.nih.gov/mesh/C14.280.123.625.440>
<http://id.nlm.nih.gov/mesh/C16.131.240.400.715.440>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:2842>
wdt:P11143 "Jervell and Lange-Nielsen syndrome"
wdt:P1193 0.000005^^xsd:decimal
wdt:P1343 wd:Q34241382
wdt:P138 Fred Lange-Nielsen
Anton Jervell
wdt:P14914 "D90647"
wdt:P1550 "90647"
wdt:P1748 "C84793"
wdt:P1995 cardiology
wdt:P2293 KCNQ1
KCNE1
wdt:P279 long QT syndrome
wdt:P2841 neonatal onset
wdt:P2888 <http://identifiers.org/doid/DOID:2842>
<http://purl.obolibrary.org/obo/DOID_2842>
<http://www.orpha.net/ORDO/Orphanet_90647>
wdt:P2892 "C0022387"
wdt:P31 type of disease
rare disease
wdt:P4317 "3048"
wdt:P486 "D029593"
wdt:P492 "220400"
"612347"
wdt:P493 "426.82"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0002441"
wdt:P557 "7249"
wdt:P6366 "2778026839"
wdt:P646 "/m/0578_n"
wdt:P6532 unconsciousness
Prolonged QTc interval
Bilateral sensorineural hearing impairment
Profound sensorineural hearing impairment
Postexertional symptom exacerbation
torsades de pointes
syncope
heart arrhythmia
seizure
ventricular fibrillation
iron deficiency anemia
wdt:P665 "H02091"
wdt:P668 "NBK1405"
wdt:P672 "C14.280.067.565.440"
"C14.280.123.625.440"
"C16.131.240.400.715.440"
wdt:P699 "DOID:2842"
wdt:P7464 "jervell-and-lange-nielsen-syndrome"
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data from SPARQL profile: Wikidata