Long Qt Syndrome 1
Disease ID: disease_node_16880
Connections displayed (default: 10).
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| Dbxref | GARD:3284, ICD10CM:I45.8, MIM:192500 |
|---|---|
| Subclassof | DOID_0050736, DOID_2843, DOID_0080578 |
| Data Source | DOID |
| Synonyms | LQT1, ventricular fibrillation with prolonged QT interval |
| Doid Label | long QT syndrome 1 |
| Doid Description | A long QT syndrome that has_material_basis_in domit inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4. |
| Has Material Basis In | GENO_0000147, GENO_0000930 |
| Disease Node Id | disease_node_16880 |
| Doid Id | DOID_0110644 |
| Label | Long Qt Syndrome 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Long Qt Syndrome(ID:disease_node_4835) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Digenic Disease(ID:disease_node_13627) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)