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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 3
5 OMIM references -
8 associated genes
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial pancreatic carcinoma

LMNA BRCA1
BRCA2
CDKN2A
KRAS
MANF
PALB2
SMAD4
TP53


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
LMNA
LMNA
(0.06)
(0.06)
(0.06)
BRCA1
BRCA2
PALB2



Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Familial pancreatic carcinoma
BRCA1 BRCA2 CDKN2A KRAS MANF PALB2
SMAD4 TP53



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial pancreatic carcinoma

Synonym(s):
(no synonyms)

Synonym(s):
- Familial pancreatic cancer

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic 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:
5 OMIM references -
1 MeSH reference: C535837

No signs/symptoms info available.