WormBase Tree Display for DO_term: DOID:2843
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| DOID:2843 | Name | long QT syndrome | |
|---|---|---|---|
| Status | Valid | ||
| Alternate_id | DOID:4069 | ||
| Definition | An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles). | ||
| Comment | OMIM mapping confirmed by DO. | ||
| Synonym | Exact | LQT | |
| long Q-T syndrome | |||
| Narrow | Romano-Ward syndrome | ||
| Parent | Is_a | DOID:0060036 | |
| Child | Is | DOID:2842 | |
| DOID:0050434 | |||
| DOID:0070533 | |||
| DOID:0110644 | |||
| DOID:0110645 | |||
| DOID:0110646 | |||
| DOID:0110647 | |||
| DOID:0110648 | |||
| DOID:0110649 | |||
| DOID:0110650 | |||
| DOID:0110651 | |||
| DOID:0110652 | |||
| DOID:0110653 | |||
| DOID:0110654 | |||
| DOID:0110655 | |||
| DOID:0110656 | |||
| DOID:0111701 | |||
| Disease_model_annotation | WBDOannot00000063 | ||
| WBDOannot00000064 | |||
| WBDOannot00000527 | |||
| Attribute_of | Gene_by_biology | WBGene00015303 | |
| WBGene00006830 | |||
| WBGene00002235 | |||
| WBGene00002233 | |||
| Gene_by_orthology | WBGene00002235 | ||
| WBGene00006062 | |||
| WBGene00006780 | |||
| WBGene00006830 | |||
| Disease_model_genotype | WBGenotype00000018 |
