ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Hereditary thrombocytosis with transverse limb defect

Myelofibrosis with myeloid metaplasia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	THPO	(0.62)	MPL

Citations in the biomedical literature:

Hereditary thrombocytosis with transverse limb defect		Myelofibrosis with myeloid metaplasia
	Synonym(s): - Familial thrombocytosis with transverse limb defect		Synonym(s): - Agnogenic myeloid metaplasia - Idiopathic myelofibrosis - Myelosclerosis with myeloid metaplasia - Primary myelofibrosis

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.