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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Squamous cell carcinoma of head and neck

LMNA ING1
ING3
PTEN
TNFRSF10B


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.63)
ING1



Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Squamous cell carcinoma of head and neck
ING1 ING3 PTEN TNFRSF10B



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Squamous cell carcinoma of head and neck

Synonym(s):
(no synonyms)

Synonym(s):
- HNSCC
- Head and neck squamous cell carcinoma

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

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:
1 OMIM reference -
1 MeSH reference: C535575

No signs/symptoms info available.