Disease #02984 (CAKUT1;RHDNS1 (kidney and urinary tract, anomalies, congenital, susceptibility to, type 1 (CAKUT-1, renal hypodysplasia, nonsyndromic, type 1 (RHDNS-1))), OMIM:610805)
| Official abbreviation |
CAKUT1;RHDNS1 |
| Name |
kidney and urinary tract, anomalies, congenital, susceptibility to, type 1 (CAKUT-1, renal hypodysplasia, nonsyndromic, type 1 (RHDNS-1)) |
| OMIM ID |
610805 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
DSTYK |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
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