Preferred Name |
Jervell and Lange-Nielsen syndrome 1 |
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Synonyms |
JLNS1 |
|
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. |
|
ID |
http://identifiers.org/omim/220400 |
|
altLabel |
JLNS1 |
|
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. |
|
id |
OMIM:220400 |
|
notation |
OMIM:220400 |
|
prefLabel |
Jervell and Lange-Nielsen syndrome 1 |
|
subClassOf |
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