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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
2 signs/symptoms
X-linked severe congenital neutropenia
Neutrophil immunodeficiency syndrome

WAS RAC2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
WAS
(0.56)
RAC2



Citations in the biomedical literature:


X-linked severe congenital neutropenia
WAS
Neutrophil immunodeficiency syndrome
RAC2



X-linked severe congenital neutropenia
Neutrophil immunodeficiency syndrome

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

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

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:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: unknown

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


COMMON
SIGNS
- Polynuclear cells / neutrophils anomalies / neutropenia


X-linked severe congenital neutropenia
Neutrophil immunodeficiency syndrome

Very frequent
- Agammaglobulinemia / hypogammaglobulinemia / B-cell deficiency
- X-linked recessive inheritance



Very frequent
- Immunodeficiency / increased susceptibility to infections / recurrent infections