Myeloid or lymphoid neoplasms with FGFR1 abnormalities (Q39187): Difference between revisions
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Neoplasias hematológicas caracterizadas pelo rearranjo do gene FGFR1, resultando em translocações com um ponto de quebra 8p11. Os pacientes podem apresentar neoplasia mieloproliferativa, leucemia mieloide aguda, linfoma / leucemia linfoblástica de linhagem de células T ou B ou leucemia aguda de fenótipo misto. | |||
| description / en | description / en | ||
Hematologic neoplasms characterised by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint. Patients may present with a myeloproliferative neoplasm, acute myeloid leukaemia, lymphoblastic lymphoma/leukaemia of T or B-cell lineage, or acute leukaemia of mixed phenotype. | |||
Revision as of 04:31, 13 August 2026
Hematologic neoplasms characterised by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint. Patients may present with a myeloproliferative neoplasm, acute myeloid leukaemia, lymphoblastic lymphoma/leukaemia of T or B-cell lineage, or acute leukaemia of mixed phenotype.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 2A52 |
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| English | Myeloid or lymphoid neoplasms with FGFR1 abnormalities |
Hematologic neoplasms characterised by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint. Patients may present with a myeloproliferative neoplasm, acute myeloid leukaemia, lymphoblastic lymphoma/leukaemia of T or B-cell lineage, or acute leukaemia of mixed phenotype. |
