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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
3 associated genes
No signs/symptoms info
Glanzmann thrombasthenia
Idiopathic hypereosinophilic syndrome

ITGA2B FIP1L1
ITGB3 PDGFRA
PDGFRB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ITGB3
ITGB3
(0.74)
(0.74)
PDGFRA
PDGFRB



Citations in the biomedical literature:


Glanzmann thrombasthenia
ITGA2B ITGB3
Idiopathic hypereosinophilic syndrome
FIP1L1 PDGFRA PDGFRB



Glanzmann thrombasthenia
Idiopathic hypereosinophilic syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

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

No signs/symptoms info available.