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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Nodular urticaria pigmentosa
Idiopathic hypereosinophilic syndrome

KIT FIP1L1
PDGFRA
PDGFRB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIT
(0.63)
PDGFRA



Citations in the biomedical literature:


Nodular urticaria pigmentosa
KIT
Idiopathic hypereosinophilic syndrome
FIP1L1 PDGFRA PDGFRB



Nodular urticaria pigmentosa
Idiopathic hypereosinophilic syndrome

Classification (Orphanet):
- Rare allergic disease
- Rare hematologic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

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

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.