Disease #02948 (ARVD11 (dysplasia, ventricular, right, arrhythmogenic, type 11 (ARVD-11)), OMIM:610476)
Official abbreviation |
ARVD11 |
Name |
dysplasia, ventricular, right, arrhythmogenic, type 11 (ARVD-11) |
OMIM ID |
610476 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
DSC2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|