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Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Hereditary breast cancer
6 OMIM references -
4 associated genes
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Hereditary breast cancer

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LMNA
LMNA
(0.06)
(0.06)
BRCA1
BRCA2


Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Hereditary breast cancer
BRCA1 BRCA2 KLLN XRCC2



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Hereditary breast cancer

Synonym(s):
(no synonyms)

Synonym(s):
- Familial breast cancer
- Familial breast carcinoma
- Hereditary breast carcinoma
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
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.