ODCs

Click node...

1 OMIM reference -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

1 OMIM reference -
1 associated gene
7 signs/symptoms

Familial multiple meningioma

Beta-thalassemia - X-linked thrombocytopenia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SMARCB1 SMARCE1	(0.75) (0.75)	GATA1 GATA1

Citations in the biomedical literature:

Familial multiple meningioma		Beta-thalassemia - X-linked thrombocytopenia
	Synonym(s): (no synonyms)		Synonym(s): - XLTT

	Classification (Orphanet): - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - 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: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: x-linked recessive

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

Beta-thalassemia - X-linked thrombocytopenia
	Very frequent - Anaemia - Hemoglobinosis / hemoglobinopathy - Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding - Platelets function anomaly - Splenomegaly - Thrombocytopenia / thrombopenia - X-linked recessive inheritance
Familial multiple meningioma
(no data available)