Disease #03344 (LQT13 (QT syndrome, long, type 13 (LQT-13)), OMIM:613485)
| Official abbreviation |
LQT13 |
| Name |
QT syndrome, long, type 13 (LQT-13) |
| OMIM ID |
613485 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
KCNJ5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|