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loading...| Preferred Name | Myeloproliferative Disorders [Disease/Finding] | |
| Synonyms |
|
|
| ID |
http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002082 |
|
| code |
C4342 |
|
| Display_Name |
Myeloproliferative Disorders |
|
| imported from | ||
| label |
Myeloproliferative Disorders [Disease/Finding] |
|
| MeSH_CUI |
M0014332 |
|
| MeSH_Definition |
Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE. |
|
| MeSH_DUI |
D009196 |
|
| MeSH_Name |
Myeloproliferative Disorders |
|
| NUI |
N0000002082 |
|
| prefixIRI |
NDF-RT:N0000002082 |
|
| prefLabel |
Myeloproliferative Disorders [Disease/Finding] |
|
| RxNorm_CUI |
1022355 |
|
| SNOMED_CID |
128925001 414792005 414794006 |
|
| UMLS_CUI |
C0027022 |
|
| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002082 | ODAE | SAME_URI | |
| http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002082 | CIDO | SAME_URI | |
| http://purl.bioontology.org/ontology/NDFRT/N0000002082 | NDFRT | LOOM | |
| http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002082 | ODAE | LOOM | |
| http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002082 | CIDO | LOOM |