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Disease Ontology Browser
essential thrombocythemia (DOID:2224)
Alliance: disease page
Synonyms: Essential thrombocythaemia; familial thrombocytosis; hemorrhagic thrombocythemia; hereditary thrombocythemia; primary Thrombocytosis
Alt IDs: OMIM:187950, OMIM:601977, OMIM:614521, ICD10CM:D47.3, ICD9CM:238.71, MESH:D013920, NCI:C3407, ORDO:3318, ORDO:71493, UMLS_CUI:C0040028
Definition: A myeloproliferative neoplasm that is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage and that results_in the overproduction of platelets.

Disease References using Mouse Models (10)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.17
The Jackson Laboratory