1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0112266 | nephrotic syndrome type 23 | A familial nephrotic syndrome characterized by onset of proteinuria in the first or second decade of life, mesangial hypercellularity, focal segmental glomerulosclerosis, and effacement of podocyte foot processes that has_material_basis_in homozygous or compound heterozygous mutation in the KIRREL1 gene on chromosome 1q23.1. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:18 | urinary system disease | A disease of anatomical entity that is located_in kidney, ureter, bladder and urethra. |
