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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
Adult-onset distal myopathy due to VCP mutation
1 associated gene
No signs/symptoms info
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Adult-onset distal myopathy due to VCP mutation

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PTPRO
(0.63)
VCP


Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO
Adult-onset distal myopathy due to VCP mutation
VCP



Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Adult-onset distal myopathy due to VCP mutation

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.