Disease #03289 (FSGS5 (glomerulosclerosis, segmental, focal, type 5 (FSGS-5)), OMIM:613237)
| Official abbreviation |
FSGS5 |
| Name |
glomerulosclerosis, segmental, focal, type 5 (FSGS-5) |
| OMIM ID |
613237 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
INF2 |
| 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) |
Individuals
|