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

NPHS1 NPHS2
NPHS2
PTPRO


COMMON
GENES
NPHS2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NPHS1
(0.95)
NPHS2



Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO
Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes



Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes

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:
2 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.