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
|