ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

3 OMIM references -
5 associated genes
No signs/symptoms info

Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency

Idiopathic aplastic anemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	IFNGR1	(0.9)	IFNG

Citations in the biomedical literature:

Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency		Idiopathic aplastic anemia
	Synonym(s): - Autosomal dominant MSMD due to partial IFNgammaR1 deficiency - Autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency - Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency		Synonym(s): - Bone marrow failure

	Classification (Orphanet): - Rare genetic disease - Rare immune disease		Classification (Orphanet): - 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: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: adult Type of inheritance: unknown

	External references: No OMIM references No MeSH references		External references: 3 OMIM references - 1 MeSH reference: C538494

No signs/symptoms info available.