10 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:1287 | cardiovascular system disease | A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis. |
| DOID:114 | heart disease | A cardiovascular system disease that involves the heart. |
| DOID:0060118 | thoracic disease | A disease of anatomical entity that is located_in the thoracic cavity. |
| DOID:0050177 | monogenic disease | A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. |
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
| DOID:10273 | heart conduction disease | A cardiovascular system disease that involves the heart's electrical conduction system. |
| DOID:0060674 | catecholaminergic polymorphic ventricular tachycardia | A heart conduction disease characterized by adrenergically induced ventricular tachycardia manifesting as syncope and sudden death during exercise, stress or catecholamine infusion without the presence of structural cardiac abnormalities. |
| DOID:0060676 | catecholaminergic polymorphic ventricular tachycardia 2 | A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the CASQ2 gene on chromosome 1p13. |
9 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0060674 | DOID:0060676 |
| is_a | DOID:4 | DOID:0060676 |
| is_a | DOID:10273 | DOID:0060676 |
| is_a | DOID:0050177 | DOID:0060676 |
| is_a | DOID:0060118 | DOID:0060676 |
| is_a | DOID:7 | DOID:0060676 |
| is_a | DOID:114 | DOID:0060676 |
| is_a | DOID:1287 | DOID:0060676 |
| is_a | DOID:630 | DOID:0060676 |
