Long Qt Syndrome 16
Disease ID: disease_node_16875
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| Dbxref | MIM:618782 |
|---|---|
| Subclassof | DOID_0050736, DOID_2843 |
| Data Source | DOID |
| Synonyms | LQT16 |
| Doid Label | long QT syndrome 16 |
| Doid Description | A long QT syndrome characterized by perinatal onset of markedly prolonged corrected QT (QTc) interval, 2:1 atrioventricular (AV) block, and bradycardia or ventricular tachycardia (torsades de pointes) that has_material_basis_in heterozygous mutation in the CALM3 gene on chromosome 19q13.32. Syncope, cardiac arrest, and sudden death are common. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16875 |
| Doid Id | DOID_0070533 |
| Label | Long Qt Syndrome 16 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Long Qt Syndrome(ID:disease_node_4835) (Disease)