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PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Spastic paraplegia - Paget disease of bone

NPHS1 VCP
PTPRO


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 diffuse mesangial proliferation
NPHS1 PTPRO
Spastic paraplegia - Paget disease of bone
VCP



Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Spastic paraplegia - Paget disease of bone

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
(no data available)

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:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.