ORPHA:589542
Myeloid/lymphoid neoplasm associated with JAK2 rearrangement
Synonyms: Myeloid/lymphoid neoplasms with PCM1-JAK2
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood, Elderly
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Myeloid/lymphoid neoplasm associated with JAK2 rearrangement | Myeloid/lymphoid neoplasms with PCM1-JAK2 |
| fr | Tumeur myéloïde/lymphoïde associée à un réarrangement de JAK2 | Tumeur myéloïde/lymphoïde associée à PCM1-JAK2 |
| de | Myeloische/lymphatische Neoplasie mit assoziierten JAK2-Rearrangement | Myeloische/lymphatische Neoplasie mit PCM1-JAK2 |
| es | Neoplasia mieloide/linfoide asociada a un reordenamiento del gen JAK2 | Neoplasia mieloide/linfoide con PCM1-JAK2 |
| it | Neoplasia mieloide/linfoide associata a riarrangiamenti in JAK2 | Neoplasia mieloide/linfoide con PCM1-JAK2 |
| nl | Myeloïd/lymfoïd neoplasma geassocieerd met JAK2-herschikking | Myeloïd/lymfoïd neoplasma met PCM1-JAK2 |
| pt | Neoplasia mieloide/linfóide associada a rearranjo JAK2 | |
| pl | Nowotwór szpikowy/limfoidalny związany z rearanżacją JAK2 | Nowotwór szpikowy/limfoidalny z PCM1-JAK2 |
| cs | Myeloidní/lymfoidní novotvar spojený s přestavbou JAK2 | = en |
| uk | Мієлоїдні/лімфоїдні новоутворення, повязані з перебудовою JAK2 | Мієлоїдні/лімфоїдні новоутворення з PCM1-JAK2 |
| zh | Myeloid/lymphoid neoplasm associated with JAK2 rearrangement | = en |
| tr | Myeloid/lymphoid neoplasm associated with JAK2 rearrangement | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D47.1 | NTBT | attributed | validated |
| ICD-11 | 2A22 | NTBT | attributed | validated |
| MONDO | 0035121 | E | validated | |
| UMLS | C5229383 | 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:168943Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | Unknown | — | Worldwide | Class only | Validated | WHO Classification of Tumours[OTHER]_ORPHANET |
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | WHO Classification of Tumours[OTHER]_ORPHANET |
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/589542
- This record as JSON: /data/d/589542.json