Cytoscape Web
Click node...


1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
2 signs/symptoms
Generalized juvenile polyposis/juvenile polyposis coli
Neutrophil immunodeficiency syndrome

BMPR1A RAC2
ENG
SMAD4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SMAD4
(0.52)
RAC2



Citations in the biomedical literature:


Generalized juvenile polyposis/juvenile polyposis coli
BMPR1A ENG SMAD4
Neutrophil immunodeficiency syndrome
RAC2



Generalized juvenile polyposis/juvenile polyposis coli
Neutrophil immunodeficiency syndrome

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
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

Neutrophil immunodeficiency syndrome

Very frequent
- Immunodeficiency / increased susceptibility to infections / recurrent infections
- Polynuclear cells / neutrophils anomalies / neutropenia



Generalized juvenile polyposis/juvenile polyposis coli

(no data available)