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Idiopathic hypereosinophilic syndrome
1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Idiopathic hypereosinophilic syndrome
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency

FIP1L1
(UniProt - OMIM)
 TYK2
(UniProt - OMIM)
PDGFRA
(UniProt - OMIM)
PDGFRB
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PDGFRB
(0.65)
TYK2


Citations in the biomedical literature:


Idiopathic hypereosinophilic syndrome
FIP1L1 PDGFRA PDGFRB
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
TYK2



Idiopathic hypereosinophilic syndrome
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- AR hyper-IgE syndrome due to TYK2 deficiency
- AR-HIES due to TYK2 deficiency
Classification (Orphanet):
- Rare hematologic 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:
(no data available)
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.