ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Familial gastric cancer

Laminopathy type Decaudain-Vigouroux

CDH1	(UniProt - OMIM)		LMNA	(UniProt - OMIM)
MUTYH	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CDH1	(0.76)	LMNA

Citations in the biomedical literature:

Familial gastric cancer		Laminopathy type Decaudain-Vigouroux
	Synonym(s): - Familial stomach cancer		Synonym(s): - Laminopathy with severe metabolic syndrome and myopathy

	Classification (Orphanet): - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: multigenic/multifactorial		Epidemiological data: (no data available)

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

No signs/symptoms info available.