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Paris-Trousseau thrombocytopenia

1 OMIM reference -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

Hereditary site-specific ovarian cancer syndrome

2 associated genes
No signs/symptoms info

Paris-Trousseau thrombocytopenia

Hereditary site-specific ovarian cancer syndrome

FLI1	(UniProt - OMIM)		BRCA1	(UniProt - OMIM)
			BRCA2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLI1	(0.75)	BRCA1

Citations in the biomedical literature:

Paris-Trousseau thrombocytopenia		Hereditary site-specific ovarian cancer syndrome

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare hematologic 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: (no data available)		Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C538617		External references: No OMIM references No MeSH references

Paris-Trousseau thrombocytopenia
	Frequent - Intellectual deficit / mental / psychomotor retardation / learning disability - Structural anomalies of the cardio-circulatory system
Hereditary site-specific ovarian cancer syndrome
(no data available)