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Paris-Trousseau thrombocytopenia

1 OMIM reference -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

Congenital mesoblastic nephroma

2 associated genes
No signs/symptoms info

Paris-Trousseau thrombocytopenia

Congenital mesoblastic nephroma

FLI1	(UniProt - OMIM)		ETV6	(UniProt - OMIM)
			NTRK3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLI1	(0.79)	ETV6

Citations in the biomedical literature:

Paris-Trousseau thrombocytopenia		Congenital mesoblastic nephroma

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): (no data available)

	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: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C538617		External references: No OMIM references 1 MeSH reference: D018201

Paris-Trousseau thrombocytopenia
	Frequent - Intellectual deficit / mental / psychomotor retardation / learning disability - Structural anomalies of the cardio-circulatory system
Congenital mesoblastic nephroma
(no data available)