ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

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

Hereditary site-specific ovarian cancer syndrome

Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism

BRCA1	(UniProt - OMIM)		BRCC3	(UniProt - OMIM)
BRCA2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	BRCA1 BRCA2	(0.88) (0.87)	BRCC3 BRCC3

Citations in the biomedical literature:

Hereditary site-specific ovarian cancer syndrome		Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism
	Synonym(s): (no synonyms)		Synonym(s): - Syndromic Moyamoya disease

	Classification (Orphanet): - Rare genetic disease - Rare gynecologic or obstetric disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare infertility - Rare neurologic disease

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

	Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: x-linked recessive

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

No signs/symptoms info available.