Thrombocythemia, Essential
Disease ID: disease_node_7389
Connections displayed (default: 10).
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| Dbxref | GARD:6594, ICD10CM:D47.3, ICD9CM:238.71, ICDO:9962/3, MESH:D013920, MIM:187950, MIM:601977, MIM:614521, NCI:C3407, ORDO:3318, ORDO:71493, SNOMEDCT_US_2023_03_01:234499005, UMLS_CUI:C0040028 |
|---|---|
| Subclassof | DOID_2226 |
| Data Source | DOID, MESH |
| Synonyms | Essential thrombocythaemia, familial thrombocytosis, hemorrhagic thrombocythemia, hereditary thrombocythemia, primary Thrombocytosis |
| Mesh Id | D013920 |
| Mesh Label | Thrombocythemia, Essential |
| Mesh Subclassof | D013922, D001778, D006474 |
| Doid Label | essential thrombocythemia |
| Doid Description | 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. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
| Has Symptom | SYMP_0000041 |
| Disease Node Id | disease_node_7389 |
| Doid Id | DOID_2224 |
| Label | Thrombocythemia, Essential |
- Outgoing r'ship
HAS_SYMPTOMto/from Hemorrhage(ID:disease_node_3837;disease_node_21127) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Myeloproliferative Neoplasm(ID:disease_node_15338) (Disease)