ODCs

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1 OMIM reference -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
7 signs/symptoms

Paris-Trousseau thrombocytopenia

Beta-thalassemia - X-linked thrombocytopenia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLI1	(0.9)	GATA1

Citations in the biomedical literature:

Paris-Trousseau thrombocytopenia		Beta-thalassemia - X-linked thrombocytopenia
	Synonym(s): (no synonyms)		Synonym(s): - XLTT

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

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: x-linked recessive

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

Paris-Trousseau thrombocytopenia		Beta-thalassemia - X-linked thrombocytopenia
	Frequent - Intellectual deficit / mental / psychomotor retardation / learning disability - Structural anomalies of the cardio-circulatory system		Very frequent - Anaemia - Hemoglobinosis / hemoglobinopathy - Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding - Platelets function anomaly - Splenomegaly - Thrombocytopenia / thrombopenia - X-linked recessive inheritance