Jump to:
loading...| Preferred Name |
Jervell and Lange-Nielsen syndrome 1 |
|
| 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 |
Create mapping