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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
2 OMIM references -
3 associated genes
No signs/symptoms info
X-linked severe congenital neutropenia
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes

WAS NPHS1
NPHS2
PTPRO


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


X-linked severe congenital neutropenia
WAS
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO



X-linked severe congenital neutropenia
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the genitourinary system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
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 minimal changes

(no data available)