Preferred Name |
Jervell and Lange-Nielsen syndrome 1 |
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Synonyms |
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Definitions |
(JLNS1): An autosomal recessive disorder characterized by congenital deafness, prolongation of the QT interval, syncopal attacks due to ventricular arrhythmias, and a high risk of sudden death. |
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ID |
http://purl.obolibrary.org/obo/OMIM_220400 |
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definition |
(JLNS1): An autosomal recessive disorder characterized by congenital deafness, prolongation of the QT interval, syncopal attacks due to ventricular arrhythmias, and a high risk of sudden death. |
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has_obo_namespace |
cell_cycle_ontology |
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id |
OMIM:220400 |
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label |
Jervell and Lange-Nielsen syndrome 1 |
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notation |
OMIM:220400 |
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prefLabel |
Jervell and Lange-Nielsen syndrome 1 |
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treeView | ||
subClassOf |
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