Cytoscape Web
Click node...

Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
2 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Isolated bone marrow mastocytosis
1 associated gene
No signs/symptoms info
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Isolated bone marrow mastocytosis

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PTPRO
(0.73)
KIT


Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO
Isolated bone marrow mastocytosis
KIT



Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Isolated bone marrow mastocytosis

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
(no data available)
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.