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Descriptor en español: |
Cromosoma Filadelfia
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Descriptor en inglés: | Philadelphia Chromosome | ||||||
Descriptor en portugués: | Cromossomo Filadélfia | ||||||
Descriptor en francés: | Chromosome Philadelphie | ||||||
Término(s) alternativo(s): |
1 Chromosomes, Ph Chromosome, Ph 1 Chromosome, Ph1 Chromosome, Philadelphia Chromosomes, Ph 1 Chromosomes, Ph1 Ph 1 Chromosome Ph 1 Chromosomes Ph1 Chromosome Ph1 Chromosomes |
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Código(s) jeráquico(s): |
A11.284.187.520.300.325.345.500 A11.284.187.520.300.505.515.500 C23.550.210.870.680 G05.360.162.520.300.325.345.700 G05.360.162.520.300.505.515.700 G05.365.590.175.870.680 |
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Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D010677 | ||||||
Nota de alcance: | An aberrant form of human CHROMOSOME 22 characterized by translocation of the distal end of chromosome 9 from 9q34, to the long arm of chromosome 22 at 22q11. It is present in the bone marrow cells of 80 to 90 per cent of patients with chronic myelocytic leukemia (LEUKEMIA, MYELOGENOUS, CHRONIC, BCR-ABL POSITIVE). |
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Calificadores permitidos: |
DE drug effects RE radiation effects |
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Indexación anterior: |
Chromosome Abnormalities (1966-1967) Chromosomes (1966-1967) Chromosomes, Human, 21-22 (1968-1985) Leukemia, Myelocytic/FG (1966-1985) |
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Nota Pública de MeSH: | 86; was see CHROMOSOMES, HUMAN, 21-22 1978-85 |
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Nota Online: | search CHROMOSOMES, HUMAN, 21-22 1978-85 |
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Nota de historia: | 86; was see CHROMOSOMES, HUMAN, 21-22 1978-85 |
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Vea también los descriptores: |
Oncogene Proteins, Fusion
MeSH | ||||||
Identificador de DeCS: | 19631 | ||||||
ID del Descriptor: | D010677 | ||||||
Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
Fecha de establecimiento: | 01/01/1986 | ||||||
Fecha de entrada: | 03/05/1985 | ||||||
Fecha de revisión: | 28/06/2016 |
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ANATOMY
Cells [A11]Cells -
ANATOMY
Cells [A11]Cells -
PHENOMENA AND PROCESSES
Genetic Phenomena [G05]Genetic Phenomena -
PHENOMENA AND PROCESSES
Genetic Phenomena [G05]Genetic Phenomena -
PHENOMENA AND PROCESSES
Genetic Phenomena [G05]Genetic Phenomena
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Philadelphia Chromosome
- Concepto preferido
UI del concepto |
M0016591 |
Nota de alcance | An aberrant form of human CHROMOSOME 22 characterized by translocation of the distal end of chromosome 9 from 9q34, to the long arm of chromosome 22 at 22q11. It is present in the bone marrow cells of 80 to 90 per cent of patients with chronic myelocytic leukemia (LEUKEMIA, MYELOGENOUS, CHRONIC, BCR-ABL POSITIVE). |
Término preferido | Philadelphia Chromosome |
Término(s) alternativo(s) |
1 Chromosomes, Ph Chromosome, Ph 1 Chromosome, Ph1 Chromosome, Philadelphia Chromosomes, Ph 1 Chromosomes, Ph1 Ph 1 Chromosome Ph 1 Chromosomes Ph1 Chromosome Ph1 Chromosomes |
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