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Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
2 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
X-linked thrombocytopenia with normal platelets
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
X-linked thrombocytopenia with normal platelets

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PTPRO
(0.68)
WAS


Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO
X-linked thrombocytopenia with normal platelets
WAS



Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
X-linked thrombocytopenia with normal platelets

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.