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Myelofibrosis with myeloid metaplasia

1 OMIM reference -
4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Benign familial chorea

2 OMIM references -
1 associated gene
2 signs/symptoms

Myelofibrosis with myeloid metaplasia

Benign familial chorea

CALR	(UniProt - OMIM)		NKX2-1	(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)	NKX2-1

Citations in the biomedical literature:

Myelofibrosis with myeloid metaplasia		Benign familial chorea
	Synonym(s): - Agnogenic myeloid metaplasia - Idiopathic myelofibrosis - Myelosclerosis with myeloid metaplasia - Primary myelofibrosis		Synonym(s): - Hereditary benign chorea

	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: 2 OMIM references - No MeSH references

Benign familial chorea
	Very frequent - Abnormal gait - Movement disorder
Myelofibrosis with myeloid metaplasia
(no data available)