Faster access than browser!Similarities between Dominance (genetics) and Trinucleotide repeat disorder
Dominance (genetics) and Trinucleotide repeat disorder have 9 things in common (in Unionpedia): Chromosome, DNA, Gene, Genetic disorder, Huntington's disease, Intellectual disability, Mutation, Trinucleotide repeat disorder, X chromosome.
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.
Chromosome and Dominance (genetics) · Chromosome and Trinucleotide repeat disorder ·
DNA
Deoxyribonucleic acid (DNA) is a thread-like chain of nucleotides carrying the genetic instructions used in the growth, development, functioning and reproduction of all known living organisms and many viruses.
DNA and Dominance (genetics) · DNA and Trinucleotide repeat disorder ·
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
Dominance (genetics) and Gene · Gene and Trinucleotide repeat disorder ·
Genetic disorder
A genetic disorder is a genetic problem caused by one or more abnormalities in the genome.
Dominance (genetics) and Genetic disorder · Genetic disorder and Trinucleotide repeat disorder ·
Huntington's disease
Huntington's disease (HD), also known as Huntington's chorea, is an inherited disorder that results in death of brain cells.
Dominance (genetics) and Huntington's disease · Huntington's disease and Trinucleotide repeat disorder ·
Intellectual disability
Intellectual disability (ID), also known as general learning disability, and mental retardation (MR), is a generalized neurodevelopmental disorder characterized by significantly impaired intellectual and adaptive functioning.
Dominance (genetics) and Intellectual disability · Intellectual disability and Trinucleotide repeat disorder ·
Mutation
In biology, a mutation is the permanent alteration of the nucleotide sequence of the genome of an organism, virus, or extrachromosomal DNA or other genetic elements.
Dominance (genetics) and Mutation · Mutation and Trinucleotide repeat disorder ·
Trinucleotide repeat disorder
Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where trinucleotide repeats in certain genes or intronsDavid W. Sanders & Clifford P. Brangwynne (2017), Nature, 546, 215–216 (08 June 2017) exceed the normal, stable threshold, which differs per gene.
Dominance (genetics) and Trinucleotide repeat disorder · Trinucleotide repeat disorder and Trinucleotide repeat disorder ·
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.
Dominance (genetics) and X chromosome · Trinucleotide repeat disorder and X chromosome ·
The list above answers the following questions
- What Dominance (genetics) and Trinucleotide repeat disorder have in common
- What are the similarities between Dominance (genetics) and Trinucleotide repeat disorder
Dominance (genetics) and Trinucleotide repeat disorder Comparison
Dominance (genetics) has 86 relations, while Trinucleotide repeat disorder has 58. As they have in common 9, the Jaccard index is 6.25% = 9 / (86 + 58).
References
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