Disease #06567 (HNFJ4 (Hyperuricemic nephropathy, familial juvenile, 4), OMIM:617056)
| Official abbreviation |
HNFJ4 |
| Name |
Hyperuricemic nephropathy, familial juvenile, 4 |
| OMIM ID |
617056 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SEC61A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
|