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Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hyperinsulinism due to INSR deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Hyperinsulinism due to INSR deficiency

NPHS1
(UniProt - OMIM)
 INSR
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)

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


Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
NPHS1 PTPRO
Hyperinsulinism due to INSR deficiency
INSR



Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Hyperinsulinism due to INSR deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- Hyperinsulinemic hypoglycemia due to INSR deficiency
- Hyperinsulinemic hypoglycemia due to insulin receptor deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.