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Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Hereditary breast cancer
6 OMIM references -
4 associated genes
No signs/symptoms info
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Hereditary breast cancer

BRCA2
(UniProt - OMIM)
 BRCA1
(UniProt - OMIM)
BRCA2
(UniProt - OMIM)
KLLN
(UniProt - OMIM)
XRCC2
(UniProt - OMIM)

COMMON
GENES 		BRCA2
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
BRCA2
(0.9)
BRCA1


Citations in the biomedical literature:


Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
BRCA2
Hereditary breast cancer
BRCA1 KLLN XRCC2



Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Hereditary breast cancer

Synonym(s):
(no synonyms)

Synonym(s):
- Familial breast cancer
- Familial breast carcinoma
- Hereditary breast carcinoma
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
6 OMIM references -
No MeSH references
No signs/symptoms info available.