ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Familial gastric cancer

Myeloid neoplasm associated with FGFR1 rearrangement

CDH1	(UniProt - OMIM)		FGFR1	(UniProt - OMIM)
MUTYH	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CDH1	(0.63)	FGFR1

Citations in the biomedical literature:

Familial gastric cancer		Myeloid neoplasm associated with FGFR1 rearrangement
	Synonym(s): - Familial stomach cancer		Synonym(s): - 8p11 myeloproliferative syndrome - Stem cell leukemia/lymphoma

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

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

	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: 1 OMIM reference - No MeSH references

No signs/symptoms info available.