ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Philadelphia Chromosome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 21-22 and Y ∟ Chromosomes, Human, Pair 22 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 6-12 and X ∟ Chromosomes, Human, Pair 9 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Intracellular Space ∟ Cell Nucleus ∟ Cell Nucleus Structures ∟ Intranuclear Space ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 21-22 and Y ∟ Chromosomes, Human, Pair 22 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Intracellular Space ∟ Cell Nucleus ∟ Cell Nucleus Structures ∟ Intranuclear Space ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 6-12 and X ∟ Chromosomes, Human, Pair 9 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Intracellular Space ∟ Cytoplasm ∟ Cytoplasmic Structures ∟ Organelles ∟ Cell Nucleus ∟ Cell Nucleus Structures ∟ Intranuclear Space ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 21-22 and Y ∟ Chromosomes, Human, Pair 22 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Intracellular Space ∟ Cytoplasm ∟ Cytoplasmic Structures ∟ Organelles ∟ Cell Nucleus ∟ Cell Nucleus Structures ∟ Intranuclear Space ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 6-12 and X ∟ Chromosomes, Human, Pair 9 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Chromosome Aberrations ∟ Translocation, Genetic ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Genetic Processes ∟ Mutagenesis ∟ Translocation, Genetic ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 21-22 and Y ∟ Chromosomes, Human, Pair 22 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 6-12 and X ∟ Chromosomes, Human, Pair 9 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Chromosome Aberrations ∟ Translocation, Genetic ∟ Philadelphia Chromosome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 21-22 and Y ∟ Chromosomes, Human, Pair 22 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 6-12 and X ∟ Chromosomes, Human, Pair 9 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Intracellular Space ∟ Cell Nucleus ∟ Cell Nucleus Structures ∟ Intranuclear Space ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 21-22 and Y ∟ Chromosomes, Human, Pair 22 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Intracellular Space ∟ Cell Nucleus ∟ Cell Nucleus Structures ∟ Intranuclear Space ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 6-12 and X ∟ Chromosomes, Human, Pair 9 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Intracellular Space ∟ Cytoplasm ∟ Cytoplasmic Structures ∟ Organelles ∟ Cell Nucleus ∟ Cell Nucleus Structures ∟ Intranuclear Space ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 21-22 and Y ∟ Chromosomes, Human, Pair 22 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Cells ∟ Cellular Structures ∟ Intracellular Space ∟ Cytoplasm ∟ Cytoplasmic Structures ∟ Organelles ∟ Cell Nucleus ∟ Cell Nucleus Structures ∟ Intranuclear Space ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 6-12 and X ∟ Chromosomes, Human, Pair 9 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Chromosome Aberrations ∟ Translocation, Genetic ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Genetic Processes ∟ Mutagenesis ∟ Translocation, Genetic ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 21-22 and Y ∟ Chromosomes, Human, Pair 22 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Chromosomes ∟ Chromosomes, Mammalian ∟ Chromosomes, Human ∟ Chromosomes, Human, 6-12 and X ∟ Chromosomes, Human, Pair 9 ∟ Philadelphia Chromosome Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Chromosome Aberrations ∟ Translocation, Genetic ∟ Philadelphia Chromosome Chromosomes, Human, Pair 22 > Chromosomes, Human, 21-22 and Y > Chromosomes, Human > Chromosomes, Mammalian > Chromosomes > Cellular Structures > Cells > Medical Subject Headings (MeSH) Chromosomes, Human, Pair 9 > Chromosomes, Human, 6-12 and X > Chromosomes, Human > Chromosomes, Mammalian > Chromosomes > Cellular Structures > Cells > Medical Subject Headings (MeSH) Chromosomes, Human, Pair 22 > Chromosomes, Human, 21-22 and Y > Chromosomes, Human > Chromosomes, Mammalian > Chromosomes > Intranuclear Space > Cell Nucleus Structures > Cell Nucleus > Intracellular Space > Cellular Structures > Cells > Medical Subject Headings (MeSH) Chromosomes, Human, Pair 9 > Chromosomes, Human, 6-12 and X > Chromosomes, Human > Chromosomes, Mammalian > Chromosomes > Intranuclear Space > Cell Nucleus Structures > Cell Nucleus > Intracellular Space > Cellular Structures > Cells > Medical Subject Headings (MeSH) Chromosomes, Human, Pair 22 > Chromosomes, Human, 21-22 and Y > Chromosomes, Human > Chromosomes, Mammalian > Chromosomes > Intranuclear Space > Cell Nucleus Structures > Cell Nucleus > Organelles > Cytoplasmic Structures > Cytoplasm > Intracellular Space > Cellular Structures > Cells > Medical Subject Headings (MeSH) Chromosomes, Human, Pair 9 > Chromosomes, Human, 6-12 and X > Chromosomes, Human > Chromosomes, Mammalian > Chromosomes > Intranuclear Space > Cell Nucleus Structures > Cell Nucleus > Organelles > Cytoplasmic Structures > Cytoplasm > Intracellular Space > Cellular Structures > Cells > Medical Subject Headings (MeSH) Translocation, Genetic > Chromosome Aberrations > Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Translocation, Genetic > Mutagenesis > Genetic Processes > Medical Subject Headings (MeSH) Chromosomes, Human, Pair 22 > Chromosomes, Human, 21-22 and Y > Chromosomes, Human > Chromosomes, Mammalian > Chromosomes > Genetic Structures > Medical Subject Headings (MeSH) Chromosomes, Human, Pair 9 > Chromosomes, Human, 6-12 and X > Chromosomes, Human > Chromosomes, Mammalian > Chromosomes > Genetic Structures > Medical Subject Headings (MeSH) Translocation, Genetic > Chromosome Aberrations > Pathologic Processes > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
History note:	Chromosome Abnormalities (1966-1967) \| Chromosomes (1966-1967) \| Chromosomes, Human, 21-22 (1968-1985) \| Leukemia, Myelocytic/FG (1966-1985)X
historyNote*:	86; was see CHROMOSOMES, HUMAN, 21-22 1978-85 X
onlineNote*:	search CHROMOSOMES, HUMAN, 21-22 1978-85 X
publicMeSHNote*:	86; was see CHROMOSOMES, HUMAN, 21-22 1978-85 X
Scope note:	An aberrant form of human CHROMOSOME 22 characterized by translocation of genetic material from chromosome 22, usually to the long arms of chromosome 9. It is present in the bone marrow cells of 80 to 90 per cent of patients with chronic myelocytic leukemia (LEUKEMIA, MYELOID, CHRONIC). X
activeMeSHYear*:	2005 \| 2006 \| 2007X
dateCreated*:	1985-05-03X
dateEstablished*:	1986-01-01X
dateRevised*:	2004-07-13X
recordAuthorizer*:	sjnX
recordMaintainer*:	sjnX
recordOriginator*:	AEPX
Related term:	Oncogene Proteins, Fusion X
Type:	Concept X
URI:	X
Labels and equivalent concepts:	Philadelphia-kromosomi (fi) Ph-kromosomi (fi, replaced) Kromosomi, Philadelphia- (fi, replaced) Philadelphiakromosom (sv) Ph1-kromosom (sv, replaced) Ph1 Chromosome (en, replaced) Ph 1 Chromosome (en, replaced) X
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