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1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
Idiopathic hypereosinophilic syndrome
Macrocephaly-autism syndrome

FIP1L1 PTEN
PDGFRA
PDGFRB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PDGFRB
PDGFRA
(0.85)
(0.63)
PTEN
PTEN



Citations in the biomedical literature:


Idiopathic hypereosinophilic syndrome
FIP1L1 PDGFRA PDGFRB
Macrocephaly-autism syndrome
PTEN



Idiopathic hypereosinophilic syndrome
Macrocephaly-autism syndrome

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

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: autosomal dominant

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

No signs/symptoms info available.