NPHS1
| Deellabo: | PGD DNA |
| Gen (Gen Code): | NPHS1 |
| Aliases Gen: | CNF, NPHN, nephrin |
| Gen ID (NCBI): | 4868 |
| OMIM Gen ID: | 602716 |
| Chromosomale locatie: | 19q13.1 |
| Genetische aandoening / Analyse: | Nefrotisch syndroom type 1 |
| OMIM aandoening ID: | 256300 |
| Overerving: | AR |
| Aliases aandoening: | NEPHROTIC SYNDROME, TYPE 1; NPHS1 FINNISH CONGENITAL NEPHROSIS; CNF NEPHROTIC SYNDROME, CONGENITAL |