Disease #00220 (CPVT2 (VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2), OMIM:611938)
| Official abbreviation |
CPVT2 |
| Name |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2 |
| OMIM ID |
611938 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CASQ2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-09-09 10:42:54 +00:00 (UTC) |
| Date last edited |
N/A |
|
