ORPHA:98274
Myeloproliferative neoplasm
Synonyms: MPD · MPN · Myeloproliferative disorder
- Type
- Clinical group
- Group
- Group of disorders
- Age of onset
- All ages
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Myeloproliferative neoplasm | MPD · MPN · Myeloproliferative disorder |
| fr | Néoplasie myéloproliférative | MPD · MPN · Maladie myloproliférative chronique · NMP |
| de | Myeloproliferative Neoplasie | MPD · MPN · Myeloproliferative Störung |
| es | Neoplasia mieloproliferativa | MPD · MPN · Trastorno mieloproliferativo |
| it | Neoplasia mieloproliferativa | Disturbo mieloproliferativo · MPD · MPN |
| nl | Myeloproliferatief neoplasma | MPD · MPN · Myeloproliferatieve stoornis |
| pt | Doença mieloproliferativa crónica | |
| pl | Nowotwór mieloproliferacyjny | MPD · MPN · Zaburzenie mieloproliferacyjne |
| cs | Myeloproliferativní neoplázie | MPD · MPN · Myeloproliferativní choroba |
| uk | Мієлопроліферативне новоутворення | EDS · MPN · Мієлопроліферативний розлад |
| zh | 骨髓增殖性肿瘤 | 骨髓增生病 |
| tr | Miyeloproliferatif neoplazm | MPD · MPN · Miyeloproliferatif bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020076 | E | validated | |
| MeSH | D009196 | E | validated | |
| UMLS | C0027022 | E | validated | |
| GARD | 9319 | E | validated | |
| MedDRA | 10077465 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:171895Myeloid hemopathy
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
Children (12):
- ORPHA:48828014q32 duplication syndrome
- ORPHA:168940Chronic eosinophilic leukemia
- ORPHA:521Chronic myeloid leukemia
- ORPHA:86830Chronic myeloproliferative disease, unclassifiable
- ORPHA:86829Chronic neutrophilic leukemia
- ORPHA:3318Essential thrombocythemia
- ORPHA:480851Hereditary thrombocytopenia with early-onset myelofibrosis
- ORPHA:168956Hypereosinophilic syndrome
- ORPHA:729Polycythemia vera
- ORPHA:824Primary myelofibrosis
- ORPHA:675775Severe congenital myelofibrosis-pancytopenia-intellectual disability-neurologic and ophthalmic abnormalities syndrome
- ORPHA:420611Transient myeloproliferative syndrome
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 3.07 / 100 000 | Europe | Value and class | Validated | RARECARE surveillance of rare cancers in Europe[OTHER] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98274
- This record as JSON: /data/d/98274.json