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Myelofibrosis with myeloid metaplasia
1 OMIM reference -
4 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
Myelofibrosis with myeloid metaplasia
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency

CALR
(UniProt - OMIM)
 IFNGR2
(UniProt - OMIM)
JAK2
(UniProt - OMIM)
MPL
(UniProt - OMIM)
TET2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
JAK2
(0.92)
IFNGR2


Citations in the biomedical literature:


Myelofibrosis with myeloid metaplasia
CALR JAK2 MPL TET2
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
IFNGR2



Myelofibrosis with myeloid metaplasia
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency

Synonym(s):
- Agnogenic myeloid metaplasia
- Idiopathic myelofibrosis
- Myelosclerosis with myeloid metaplasia
- Primary myelofibrosis
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
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Neoplasms -
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: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.