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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Autosomal codominant severe lipodystrophic laminopathy

BRCA2 LMNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
BRCA2
(0.06)
LMNA



Citations in the biomedical literature:


Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
BRCA2
Autosomal codominant severe lipodystrophic laminopathy
LMNA



Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Autosomal codominant severe lipodystrophic laminopathy

Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare skin disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.