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MedlinePlus Health Topics
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/MEDLINEPLUS/C0022387
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0022387
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| Preferred Name | Cardio-auditory-syncope syndrome |
| Definitions |
Jervell and Lange-Nielsen syndrome is a condition that causes profound hearing loss from birth and a disruption of the heart's normal rhythm (arrhythmia). This disorder is a form of long QT syndrome, which is a heart condition that causes the heart (cardiac) muscle to take longer than usual to recharge between beats. Beginning in early childhood, the irregular heartbeats increase the risk of fainting (syncope) and sudden death.
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| Synonyms |
Jervell and Lange-Nielsen syndrome
Prolonged QT interval in EKG and sudden death
JLNS
Cardioauditory syndrome of Jervell and Lange-Nielsen
Jervell-Lange Nielsen syndrome
Deafness, congenital, and functional heart disease
Surdo-cardiac syndrome
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | Jervell and Lange-Nielsen syndrome is a condition that causes profound hearing loss from birth and a disruption of the heart's normal rhythm (arrhythmia). This disorder is a form of long QT syndrome, which is a heart condition that causes the heart (cardiac) muscle to take longer than usual to recharge between beats. Beginning in early childhood, the irregular heartbeats increase the risk of fainting (syncope) and sudden death. |
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| altLabel |
Jervell and Lange-Nielsen syndrome
Prolonged QT interval in EKG and sudden death
JLNS
Cardioauditory syndrome of Jervell and Lange-Nielsen
Jervell-Lange Nielsen syndrome
Deafness, congenital, and functional heart disease
Surdo-cardiac syndrome
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| prefLabel | Cardio-auditory-syncope syndrome
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| Associated condition of | |
| DB XR ID | GTR:C0022387~GTR:C2676723~GTR:C4551509~ICD-10-CM:I45.81~MeSH:D029593~OMIM:220400~OMIM:612347~SNOMED CT:373905003
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| Inheritance | ar:Autosomal recessive
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| type | |
| tui | T047
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| notation | C0022387
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| Semantic type UMLS property | |
| cui | C0022387
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