Cytoscape Web
Click node...

Craniopharyngioma
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary site-specific ovarian cancer syndrome
2 associated genes
No signs/symptoms info
Craniopharyngioma
Hereditary site-specific ovarian cancer syndrome

BRAF
(UniProt - OMIM)
 BRCA1
(UniProt - OMIM)
CTNNB1
(UniProt - OMIM)
 BRCA2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CTNNB1
(0.68)
BRCA1


Citations in the biomedical literature:


Craniopharyngioma
BRAF CTNNB1
Hereditary site-specific ovarian cancer syndrome
BRCA1 BRCA2



Craniopharyngioma
Hereditary site-specific ovarian cancer syndrome

Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
1 MeSH reference: D003397
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.