ODCs

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2 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
2 signs/symptoms

Peripheral primitive neuroectodermal tumor

Paris-Trousseau thrombocytopenia

ERG	(UniProt - OMIM)		FLI1	(UniProt - OMIM)
FLI1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ERG	(0.52)	FLI1

Citations in the biomedical literature:

Peripheral primitive neuroectodermal tumor		Paris-Trousseau thrombocytopenia
	Synonym(s): - PPNET - Peripheral PNET		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare bone disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare hematologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

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

Paris-Trousseau thrombocytopenia
	Frequent - Intellectual deficit / mental / psychomotor retardation / learning disability - Structural anomalies of the cardio-circulatory system
Peripheral primitive neuroectodermal tumor
(no data available)