ORPHA:86851
Acute leukemia of ambiguous lineage
Synonyms: Acute leukemia of indeterminate lineage · Hybrid acute leukemia · Mixed lineage acute leukemia
- Type
- Category
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acute leukemia of ambiguous lineage | Acute leukemia of indeterminate lineage · Hybrid acute leukemia · Mixed lineage acute leukemia |
| fr | Leucémie aiguë de lignée ambiguë | Leucémie aiguë de lignée intermédiaire · Leucémie aiguë de lignée mixte · Leucémie aiguë hybride |
| de | Leukämie, akute, gemischter Linienzugehörigkeit | Akute Hybrid-Leukämie · Leukämie, akute mit gemischtem Phänotyp · Mixed-Lineage Leukämie, akute |
| es | Leucemia aguda de línea ambigua | Leucemia aguda de línea indeterminada · Leucemia aguda de línea mixta · Leucemia aguda híbrida |
| it | Leucemia acuta con lineage ambiguo | Leucemia acuta a fenotipo misto · Leucemia acuta a linee miste · Leucemia acuta con lineage sconosciuto · Leucemia ibrida acuta |
| nl | Acute leukemie van ambigue oorsprong | Acute leukemie van gemengde oorsprong · Acute leukemie van onbepaalde oorsprong · Hybride acute leukemie |
| pt | Leucemia aguda de linhagem ambígua | |
| pl | Ostra białaczka z niezidentyfikowanej linii | Ostra białaczka o mieszanym fenotypie · Ostra białaczka z linii mieszanej · Ostra białaczka z linii nieokreślonej |
| cs | Akutní leukémie nejednoznačné linie | Hybridní akutní leukémie · Akutní leukémie se smíšenou linií · Akutní leukémie se smíšeným fenotypem · Akutní leukémie neurčitého původu |
| uk | Гострий лейкоз неясного походження | Гострий лейкоз невизначеного походження · Гібридна гостра лейкемія · Гострий лейкоз змішаного походження |
| zh | 系列不明白血病 | 未定系列的急性白血病 |
| tr | Belirsiz soy hattının akut lösemisi | Hibrit akut lösemi · Karma kökenli akut lösemi · Belirsiz kökenli akut lösemi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 601626 | NTBT | validated | |
| ICD-10 | C95.0 | E | specific | validated |
| ICD-11 | 2A61 | E | specific | validated |
| MONDO | 0019460 | E | validated | |
| UMLS | C1301357 | E | validated | |
| GARD | 8638 | 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
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/86851
- This record as JSON: /data/d/86851.json