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Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome

BRCA2
(UniProt - OMIM)
 ATR
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
BRCA2
(0.63)
ATR


Citations in the biomedical literature:


Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
BRCA2
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
ATR



Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.