Disease #01463 (ADTKD1;HNFJ1;MCKD2 (kidney disease, tubulointerstitial, autosomal dominant, type 1), OMIM:162000)
| Official abbreviation |
ADTKD1;HNFJ1;MCKD2 |
| Name |
kidney disease, tubulointerstitial, autosomal dominant, type 1 |
| OMIM ID |
162000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
UMOD |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2026-04-09 10:43:37 +02:00 (CEST) |
Individuals
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