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
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