Disease #05805 (RHDA (hypodysplasia/aplasia, renal (RHDA)))
| Official abbreviation |
RHDA |
| Name |
hypodysplasia/aplasia, renal (RHDA) |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
GREB1L |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-08-07 09:59:48 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
|