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Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial renal amyloidosis due to Apolipoprotein AI variant
1 associated gene
No signs/symptoms info
Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial renal amyloidosis due to Apolipoprotein AI variant

APOL1
(UniProt - OMIM)
 APOA1
(UniProt - OMIM)
NPHS2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
APOL1
(0.68)
APOA1


Citations in the biomedical literature:


Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
APOL1 NPHS2
Familial renal amyloidosis due to Apolipoprotein AI variant
APOA1



Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial renal amyloidosis due to Apolipoprotein AI variant

Synonym(s):
- Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis
Synonym(s):
- Apolipoprotein AI amyloidosis
- Familial amyloid nephropathy due to apolipoprotein AI variant
- Hereditary amyloid nephropathy due to apolipoprotein AI variant
- Hereditary renal amyloidosis due to apolipoprotein AI variant
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.