Faster access than browser!Similarities between Chromosome and XYY syndrome
Chromosome and XYY syndrome have 20 things in common (in Unionpedia): Aneuploidy, Barr body, Cell nucleus, Chromosomal translocation, Cytogenetics, Down syndrome, Genetic disorder, Heredity, Interphase, Joe Hin Tjio, Klinefelter syndrome, Metaphase, Mitosis, Mosaic (genetics), Nondisjunction, Ploidy, Triple X syndrome, Turner syndrome, X chromosome, Y chromosome.
Aneuploidy
Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for example a human cell having 45 or 47 chromosomes instead of the usual 46.
Aneuploidy and Chromosome · Aneuploidy and XYY syndrome ·
Barr body
A Barr body (named after discoverer Murray Barr) is the inactive X chromosome in a female somatic cell, rendered inactive in a process called lyonization, in those species in which sex is determined by the presence of the Y (including humans) or W chromosome rather than the diploidy of the X. The Lyon hypothesis states that in cells with multiple X chromosomes, all but one are inactivated during mammalian embryogenesis.
Barr body and Chromosome · Barr body and XYY syndrome ·
Cell nucleus
In cell biology, the nucleus (pl. nuclei; from Latin nucleus or nuculeus, meaning kernel or seed) is a membrane-enclosed organelle found in eukaryotic cells.
Cell nucleus and Chromosome · Cell nucleus and XYY syndrome ·
Chromosomal translocation
In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes.
Chromosomal translocation and Chromosome · Chromosomal translocation and XYY syndrome ·
Cytogenetics
Cytogenetics is a branch of genetics that is concerned with how the chromosomes relate to cell behaviour, particularly to their behaviour during mitosis and meiosis.
Chromosome and Cytogenetics · Cytogenetics and XYY syndrome ·
Down syndrome
Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21.
Chromosome and Down syndrome · Down syndrome and XYY syndrome ·
Genetic disorder
A genetic disorder is a genetic problem caused by one or more abnormalities in the genome.
Chromosome and Genetic disorder · Genetic disorder and XYY syndrome ·
Heredity
Heredity is the passing on of traits from parents to their offspring, either through asexual reproduction or sexual reproduction, the offspring cells or organisms acquire the genetic information of their parents.
Chromosome and Heredity · Heredity and XYY syndrome ·
Interphase
Interphase is the phase of the cell cycle in which a typical cell spends most of its life.
Chromosome and Interphase · Interphase and XYY syndrome ·
Joe Hin Tjio
Joe Hin Tjio (2 November 1919 – 27 November 2001), was an Indonesian-born American cytogeneticist.
Chromosome and Joe Hin Tjio · Joe Hin Tjio and XYY syndrome ·
Klinefelter syndrome
Klinefelter syndrome (KS) also known as 47,XXY or XXY, is the set of symptoms that result from two or more X chromosomes in males.
Chromosome and Klinefelter syndrome · Klinefelter syndrome and XYY syndrome ·
Metaphase
Metaphase (from the Greek μετά, "adjacent" and φάσις, "stage") is a stage of mitosis in the eukaryotic cell cycle in which chromosomes are at their second-most condensed and coiled stage (they are at their most condensed in anaphase).
Chromosome and Metaphase · Metaphase and XYY syndrome ·
Mitosis
In cell biology, mitosis is a part of the cell cycle when replicated chromosomes are separated into two new nuclei.
Chromosome and Mitosis · Mitosis and XYY syndrome ·
Mosaic (genetics)
In genetics, a mosaic, or mosaicism, involves the presence of two or more populations of cells with different genotypes in one individual, who has developed from a single fertilized egg.
Chromosome and Mosaic (genetics) · Mosaic (genetics) and XYY syndrome ·
Nondisjunction
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate properly during cell division.
Chromosome and Nondisjunction · Nondisjunction and XYY syndrome ·
Ploidy
Ploidy is the number of complete sets of chromosomes in a cell, and hence the number of possible alleles for autosomal and pseudoautosomal genes.
Chromosome and Ploidy · Ploidy and XYY syndrome ·
Triple X syndrome
Triple X syndrome, also known as trisomy X and 47,XXX, is characterized by the presence of an extra X chromosome in each cell of a female.
Chromosome and Triple X syndrome · Triple X syndrome and XYY syndrome ·
Turner syndrome
Turner syndrome (TS), also known as 45,X or 45,X0, is a condition in which a female is partly or completely missing an X chromosome.
Chromosome and Turner syndrome · Turner syndrome and XYY syndrome ·
X chromosome
The X chromosome is one of the two sex-determining chromosomes (allosomes) in many organisms, including mammals (the other is the Y chromosome), and is found in both males and females.
Chromosome and X chromosome · X chromosome and XYY syndrome ·
Y chromosome
The Y chromosome is one of two sex chromosomes (allosomes) in mammals, including humans, and many other animals.
Chromosome and Y chromosome · XYY syndrome and Y chromosome ·
The list above answers the following questions
- What Chromosome and XYY syndrome have in common
- What are the similarities between Chromosome and XYY syndrome
Chromosome and XYY syndrome Comparison
Chromosome has 240 relations, while XYY syndrome has 179. As they have in common 20, the Jaccard index is 4.77% = 20 / (240 + 179).
References
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