Disease #05215 (nephrotic syndrome, congenital, male hypergonadotropic hypogonadism, adrenal calcification with/without adrenal insufficiency)
| Official abbreviation |
- |
| Name |
nephrotic syndrome, congenital, male hypergonadotropic hypogonadism, adrenal calcification with/without adrenal insufficiency |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
SGPL1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-01-13 21:44:48 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|