ODCs

Click node...

5 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

2 associated genes
No signs/symptoms info

Periventricular nodular heterotopia

Hereditary site-specific ovarian cancer syndrome


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

Citations in the biomedical literature:

Periventricular nodular heterotopia		Hereditary site-specific ovarian cancer syndrome

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic 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: - 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: 5 OMIM references - 1 MeSH reference: D054091		External references: No OMIM references No MeSH references

No signs/symptoms info available.