Disease #01182 (ARVD1 (dysplasia, arrhythmogenic right ventricular, type 1 (ARVD-1)), OMIM:107970)
Official abbreviation |
ARVD1 |
Name |
dysplasia, arrhythmogenic right ventricular, type 1 (ARVD-1) |
OMIM ID |
107970 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
TGFB3 |
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) |
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