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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
Chronic myelomonocytic leukemia
2 associated genes
No signs/symptoms info
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Chronic myelomonocytic leukemia

NPHS1
(UniProt - OMIM)
 ETV6
(UniProt - OMIM)
NPHS2
(UniProt - OMIM)
 PDGFRB
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)

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


Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO
Chronic myelomonocytic leukemia
ETV6 PDGFRB



Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Chronic myelomonocytic leukemia

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):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
1 MeSH reference: D015477
No signs/symptoms info available.