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Idiopathic hypereosinophilic syndrome
1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Rippling muscle disease
2 OMIM references -
1 associated gene
No signs/symptoms info
Idiopathic hypereosinophilic syndrome
Rippling muscle disease

FIP1L1
(UniProt - OMIM)
 CAV3
(UniProt - OMIM)
PDGFRA
(UniProt - OMIM)
PDGFRB
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PDGFRA
PDGFRB
(0.75)
(0.75)
CAV3
CAV3


Citations in the biomedical literature:


Idiopathic hypereosinophilic syndrome
FIP1L1 PDGFRA PDGFRB
Rippling muscle disease
CAV3



Idiopathic hypereosinophilic syndrome
Rippling muscle disease

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C535685
No signs/symptoms info available.