Faster access than browser!Similarities between Aneuploidy and Human genome
Aneuploidy and Human genome have 16 things in common (in Unionpedia): Cancer, Chromosome, Chromosome 13, Chromosome 18, Chromosome 21, Down syndrome, Gamete, Karyotype, Klinefelter syndrome, Meiosis, Mosaic (genetics), Nondisjunction, Ploidy, Turner syndrome, X chromosome, Y chromosome.
Cancer
Cancer is a group of diseases involving abnormal cell growth with the potential to invade or spread to other parts of the body.
Aneuploidy and Cancer · Cancer and Human genome ·
Chromosome
A chromosome (from Ancient Greek: χρωμόσωμα, chromosoma, chroma means colour, soma means body) is a DNA molecule with part or all of the genetic material (genome) of an organism.
Aneuploidy and Chromosome · Chromosome and Human genome ·
Chromosome 13
Chromosome 13 is one of the 23 pairs of chromosomes in humans.
Aneuploidy and Chromosome 13 · Chromosome 13 and Human genome ·
Chromosome 18
Chromosome 18 is one of the 23 pairs of chromosomes in humans.
Aneuploidy and Chromosome 18 · Chromosome 18 and Human genome ·
Chromosome 21
Chromosome 21 is one of the 23 pairs of chromosomes in humans.
Aneuploidy and Chromosome 21 · Chromosome 21 and Human genome ·
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.
Aneuploidy and Down syndrome · Down syndrome and Human genome ·
Gamete
A gamete (from Ancient Greek γαμετή gamete from gamein "to marry") is a haploid cell that fuses with another haploid cell during fertilization (conception) in organisms that sexually reproduce.
Aneuploidy and Gamete · Gamete and Human genome ·
Karyotype
A karyotype is the number and appearance of chromosomes in the nucleus of a eukaryotic cell.
Aneuploidy and Karyotype · Human genome and Karyotype ·
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.
Aneuploidy and Klinefelter syndrome · Human genome and Klinefelter syndrome ·
Meiosis
Meiosis (from Greek μείωσις, meiosis, which means lessening) is a specialized type of cell division that reduces the chromosome number by half, creating four haploid cells, each genetically distinct from the parent cell that gave rise to them.
Aneuploidy and Meiosis · Human genome and Meiosis ·
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.
Aneuploidy and Mosaic (genetics) · Human genome and Mosaic (genetics) ·
Nondisjunction
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate properly during cell division.
Aneuploidy and Nondisjunction · Human genome and Nondisjunction ·
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.
Aneuploidy and Ploidy · Human genome and Ploidy ·
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.
Aneuploidy and Turner syndrome · Human genome and Turner 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.
Aneuploidy and X chromosome · Human genome and X chromosome ·
Y chromosome
The Y chromosome is one of two sex chromosomes (allosomes) in mammals, including humans, and many other animals.
Aneuploidy and Y chromosome · Human genome and Y chromosome ·
The list above answers the following questions
- What Aneuploidy and Human genome have in common
- What are the similarities between Aneuploidy and Human genome
Aneuploidy and Human genome Comparison
Aneuploidy has 105 relations, while Human genome has 206. As they have in common 16, the Jaccard index is 5.14% = 16 / (105 + 206).
References
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