Disease #00254 (RTD (dysgenesis, renal tubular (RTD)), OMIM:267430)
Official abbreviation |
RTD |
Name |
dysgenesis, renal tubular (RTD) |
OMIM ID |
267430 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
50 |
Phenotype entries for this disease |
50 |
Associated with 4 genes |
ACE, AGT, AGTR1, REN |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-10-20 21:21:05 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|