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Myelofibrosis with myeloid metaplasia
1 OMIM reference -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
1 OMIM reference -
1 associated gene
No signs/symptoms info
Myelofibrosis with myeloid metaplasia
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity

CALR
(UniProt - OMIM)
 SLC2A1
(UniProt - OMIM)
JAK2
(UniProt - OMIM)
MPL
(UniProt - OMIM)
TET2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CALR
(0.78)
SLC2A1


Citations in the biomedical literature:


Myelofibrosis with myeloid metaplasia
CALR JAK2 MPL TET2
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
SLC2A1



Myelofibrosis with myeloid metaplasia
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity

Synonym(s):
- Agnogenic myeloid metaplasia
- Idiopathic myelofibrosis
- Myelosclerosis with myeloid metaplasia
- Primary myelofibrosis
Synonym(s):
- DYT9
- Episodic choreoathetosis/spasticity
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.