ODCs

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

GrÃ¤sbeck-Imerslund disease

Hereditary site-specific ovarian cancer syndrome

AMN	(UniProt - OMIM)		BRCA1	(UniProt - OMIM)
CUBN	(UniProt - OMIM)		BRCA2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CUBN	(0.63)	BRCA1

Citations in the biomedical literature:

GrÃ¤sbeck-Imerslund disease		Hereditary site-specific ovarian cancer syndrome
	Synonym(s): - Familial megaloblastic anemia - Selective cobalamin malabsorption with proteinuria		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare gastroenterologic disease - Rare genetic disease - Rare hematologic disease - Rare renal disease		Classification (Orphanet): - Rare genetic disease - Rare gynecologic or obstetric disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.