ODCs

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

PROTEIN INTERACTIONS: 2

2 associated genes
No signs/symptoms info

Congenital valvular dysplasia

Hereditary site-specific ovarian cancer syndrome

FLNA	(UniProt - OMIM)		BRCA1	(UniProt - OMIM)
			BRCA2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA FLNA	(0.79) (0.73)	BRCA2 BRCA1

Citations in the biomedical literature:

Congenital valvular dysplasia		Hereditary site-specific ovarian cancer syndrome

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare surgical cardiac disease		Classification (Orphanet): - Rare genetic disease - Rare gynecologic or obstetric disease - Rare oncologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: sporadic		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.