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Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
2 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
2 OMIM references -
3 associated genes
No signs/symptoms info
Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes

APOL1
(UniProt - OMIM)
 NPHS1
(UniProt - OMIM)
NPHS2
(UniProt - OMIM)
 NPHS2
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)

COMMON
GENES 		NPHS2
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NPHS2
(0.95)
NPHS1


Citations in the biomedical literature:


Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
APOL1 NPHS2
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 PTPRO



Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes

Synonym(s):
- Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis
Synonym(s):
(no synonyms)
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):
- Diseases of the genitourinary system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.