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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
X-linked severe congenital neutropenia
1 OMIM reference -
1 associated gene
3 signs/symptoms
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
X-linked severe congenital neutropenia

NPHS1
(UniProt - OMIM)
 WAS
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)

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


Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
NPHS1 PTPRO
X-linked severe congenital neutropenia
WAS



Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
X-linked severe congenital neutropenia

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
X-linked severe congenital neutropenia

Very frequent
- Agammaglobulinemia / hypogammaglobulinemia / B-cell deficiency
- Polynuclear cells / neutrophils anomalies / neutropenia
- X-linked recessive inheritance



Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation

(no data available)