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Myelofibrosis with myeloid metaplasia
1 OMIM reference -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
1 associated gene
No signs/symptoms info
Myelofibrosis with myeloid metaplasia
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency

CALR
(UniProt - OMIM)
 SH2B1
(UniProt - OMIM)
JAK2
(UniProt - OMIM)
MPL
(UniProt - OMIM)
TET2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
JAK2
(0.97)
SH2B1


Citations in the biomedical literature:


Myelofibrosis with myeloid metaplasia
CALR JAK2 MPL TET2
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
SH2B1



Myelofibrosis with myeloid metaplasia
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency

Synonym(s):
- Agnogenic myeloid metaplasia
- Idiopathic myelofibrosis
- Myelosclerosis with myeloid metaplasia
- Primary myelofibrosis
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.