Cytoscape Web
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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
6 OMIM references -
4 associated genes
No signs/symptoms info
Congenital valvular dysplasia
Hereditary breast cancer

FLNA BRCA1
BRCA2
KLLN
XRCC2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FLNA
FLNA
(0.79)
(0.73)
BRCA2
BRCA1



Citations in the biomedical literature:


Congenital valvular dysplasia
FLNA
Hereditary breast cancer
BRCA1 BRCA2 KLLN XRCC2



Congenital valvular dysplasia
Hereditary breast cancer

Synonym(s):
(no synonyms)

Synonym(s):
- Familial breast cancer
- Familial breast carcinoma
- Hereditary breast carcinoma

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
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.