Disease #05768 (CVDP1 (dysplasia, valvular, cardiac, type 1), OMIM:212093)
| Official abbreviation |
CVDP1 |
| Name |
dysplasia, valvular, cardiac, type 1 |
| OMIM ID |
212093 |
| 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 |
PLD1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-06-11 15:04:05 +02:00 (CEST) |
| Date last edited |
2024-01-26 11:42:20 +01:00 (CET) |
Individuals
|