Disease #00176 (ARVD11 (ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11), OMIM:610476)
| Official abbreviation |
ARVD11 |
| Name |
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 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 |
DSG2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2023-06-29 13:08:53 +00:00 (UTC) |
| Date last edited |
N/A |
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