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Idiopathic aplastic anemia
3 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
1 associated gene
No signs/symptoms info
Idiopathic aplastic anemia
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency

IFNG
(UniProt - OMIM)
 IFNGR2
(UniProt - OMIM)
PRF1
(UniProt - OMIM)
SBDS
(UniProt - OMIM)
TERC
(OMIM)
TERT
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
IFNG
(0.75)
IFNGR2


Citations in the biomedical literature:


Idiopathic aplastic anemia
IFNG PRF1 SBDS TERC TERT
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
IFNGR2



Idiopathic aplastic anemia
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency

Synonym(s):
- Bone marrow failure
Synonym(s):
- MSMD due to complete IFNgammaR2 deficiency
- MSMD due to complete interferon gamma receptor 2 deficiency
- Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency
Classification (Orphanet):
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune 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: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: unknown
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive
External references:
3 OMIM references -
1 MeSH reference: C538494
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.