Cytoscape Web
Click node...

Congenital nephrotic syndrome, Finnish type
1 OMIM reference -
1 associated gene
9 connected diseases
4 signs/symptoms
Disease Type of connection
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
X-linked intellectual deficit, Najm type
EEM syndrome
Hypotrichosis with juvenile macular degeneration
Congenital analbuminemia
Synonym(s):
- Finnish congenital nephrosis
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: C535761
Gene symbol UniProt reference OMIM reference
NPHS1 O60500602716
Very frequent
- Autosomal recessive inheritance
- Multicystic kidney / renal dysplasia
- Nephrotic syndrome
- Proteinuria