Disease #05039 (VUR8 (reflux, vesicoureteral, type 8 (VUR8)), OMIM:615963)
| Official abbreviation |
VUR8 |
| Name |
reflux, vesicoureteral, type 8 (VUR8) |
| OMIM ID |
615963 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TNXB |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 11:00:40 +02:00 (CEST) |
| Date last edited |
2020-01-15 08:54:19 +01:00 (CET) |
Individuals
|