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
|