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Idiopathic hypereosinophilic syndrome
1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
1 associated gene
No signs/symptoms info
Idiopathic hypereosinophilic syndrome
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

FIP1L1
(UniProt - OMIM)
 TNK2
(UniProt - OMIM)
PDGFRA
(UniProt - OMIM)
PDGFRB
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PDGFRB
(0.63)
TNK2


Citations in the biomedical literature:


Idiopathic hypereosinophilic syndrome
FIP1L1 PDGFRA PDGFRB
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
TNK2



Idiopathic hypereosinophilic syndrome
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- 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 recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.