Disease #00074 (NPHS1 (nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF))), OMIM:256300)
| Official abbreviation |
NPHS1 |
| Name |
nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF)) |
| OMIM ID |
256300 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
NPHS1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-11-09 14:39:22 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|