Disease #00122 (LQT1 (Long QT Syndrome), OMIM:192500)
Official abbreviation |
LQT1 |
Name |
Long QT Syndrome |
OMIM ID |
192500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
KCNQ1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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