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
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