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loading...| Preferred Name |
Jervell and Lange Nielsen Syndrome |
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| Synonyms |
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| Definitions |
An autosomal recessive inherited syndrome caused by mutations in the KCNE1 and KCNQ1 genes. It is characterized by congenital hearing loss and arrhythmia. It is a form of long QT syndrome. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C84793 |
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| code |
C84793 |
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| Contributing_Source |
Cellosaurus |
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| definition |
An autosomal recessive inherited syndrome caused by mutations in the KCNE1 and KCNQ1 genes. It is characterized by congenital hearing loss and arrhythmia. It is a form of long QT syndrome. |
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| in_subset | ||
| label |
Jervell and Lange Nielsen Syndrome |
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| Preferred_Name |
Jervell and Lange Nielsen Syndrome |
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| prefixIRI |
NCIT:C84793 |
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| prefLabel |
Jervell and Lange Nielsen Syndrome |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0022387 |
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| subClassOf |
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