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
|