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Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
2 associated genes
10 connected diseases
No signs/symptoms info
Disease Type of connection
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
Congenital nephrotic syndrome, Finnish type
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Apolipoprotein A-I deficiency
Familial renal amyloidosis due to Apolipoprotein AI variant
Primary systemic amyloidosis
Autosomal agammaglobulinemia
Autosomal dominant nonsyndromic intellectual deficit
Synonym(s):
- Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
APOL1 O14791603743
NPHS2 Q9NP85604766
No signs/symptoms info available.