Disease #00403 (LQT1;RWS (QT syndrome, long, type 1 (LQT-1, Romano-Ward syndrome (RWS))), OMIM:192500)
Official abbreviation |
LQT1;RWS |
Name |
QT syndrome, long, type 1 (LQT-1, Romano-Ward syndrome (RWS)) |
OMIM ID |
192500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
730 |
Phenotype entries for this disease |
731 |
Associated with 1 gene |
KCNQ1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-06-06 17:34:22 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|