Disease #03951 (CPVT5 (tachycardia, ventricular, catecholaminergic polymorphic, type 5, with/without muscle weakness), OMIM:615441)
| Official abbreviation |
CPVT5 |
| Name |
tachycardia, ventricular, catecholaminergic polymorphic, type 5, with/without muscle weakness |
| OMIM ID |
615441 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
TRDN |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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