ORPHA:98277
Acute myeloid leukemia with recurrent genetic anomaly
Synonyms: AML with recurrent genetic anomaly
- Type
- Category
- Group
- Group of disorders
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acute myeloid leukemia with recurrent genetic anomaly | AML with recurrent genetic anomaly |
| fr | Leucémie aiguë myéloïde avec anomalie génétique récurrente | |
| de | Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie | AML mit rekurrenter genetischer Anomalie |
| es | Leucemia mieloide aguda con anomalía genética recurrente | LMA con anomalías genéticas recurrentes |
| it | Leucemia mieloide acuta con anomalia genetica ricorrente | AML con anomalia genetica ricorrente |
| nl | Acute myeloïde leukemie met terugkerende genetische anomalie | AML met terugkerende genetische anomalie |
| pt | Leucemia mielóide aguda com anomalias genéticas recorrentes | |
| pl | Ostra białaczka szpikowa z powracającą wadą genetyczną | AML z powracającą wadą genetyczną |
| cs | Akutní myeloidní leukémie s rekurentními genetickými abnormalitami | AML s rekurentními genetickými abnormalitami |
| uk | Гостра мієлоїдна лейкемія з рецидивуючою генетичною аномалією | ГМЛ з рецидивуючою генетичною аномалією |
| zh | 急性髓系白血病伴重现性遗传学异常 | AML伴复发性遗传学异常 |
| tr | Tekrarlayan genetik anomali ile seyreden akut miyeloid lösemi | Tekrarlayan genetik anomalili AML |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 601626 | NTBT | validated | |
| ICD-11 | 2A60.0 | E | specific | validated |
| UMLS | C4303425 | E | validated | |
| GARD | 12758 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:519Acute myeloid leukemia
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders
Children (12):
- ORPHA:98831Acute myeloid leukemia with 11q23 abnormalities
- ORPHA:319480Acute myeloid leukemia with CEBPA somatic mutations
- ORPHA:402026Acute myeloid leukemia with NPM1 somatic mutations
- ORPHA:98829Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
- ORPHA:402020Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)
- ORPHA:402014Acute myeloid leukemia with t(6;9)(p23;q34)
- ORPHA:370026Acute myeloid leukemia with t(8;16)(p11;p13) translocation
- ORPHA:102724Acute myeloid leukemia with t(8;21)(q22;q22) translocation
- ORPHA:402017Acute myeloid leukemia with t(9;11)(p22;q23)
- ORPHA:585867Acute myeloid leukemia with t(9;22)(q34.1;q11.2)
- ORPHA:520Acute promyelocytic leukemia
- ORPHA:402023Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)
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 / 1 000 000 | 0.11 / 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/98277
- This record as JSON: /data/d/98277.json