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Sporadic pheochromocytoma
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
MITF-related melanoma and renal cell carcinoma predisposition syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Sporadic pheochromocytoma
MITF-related melanoma and renal cell carcinoma predisposition syndrome

EPAS1
(UniProt - OMIM)
 MITF
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EPAS1
(0.63)
MITF


Citations in the biomedical literature:


Sporadic pheochromocytoma
EPAS1
MITF-related melanoma and renal cell carcinoma predisposition syndrome
MITF



Sporadic pheochromocytoma
MITF-related melanoma and renal cell carcinoma predisposition syndrome

Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: sporadic
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.