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  2. Autosome - Wikipedia

    en.wikipedia.org/wiki/Autosome

    Autosomal genetic disorders can arise due to a number of causes, some of the most common being nondisjunction in parental germ cells or Mendelian inheritance of deleterious alleles from parents. Autosomal genetic disorders which exhibit Mendelian inheritance can be inherited either in an autosomal dominant or recessive fashion. [7]

  3. Dominance (genetics) - Wikipedia

    en.wikipedia.org/wiki/Dominance_(genetics)

    Autosomal dominant and autosomal recessive inheritance, the two most common Mendelian inheritance patterns. An autosome is any chromosome other than a sex chromosome.. In genetics, dominance is the phenomenon of one variant of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome.

  4. Y-STR - Wikipedia

    en.wikipedia.org/wiki/Y-STR

    Y-STRs are taken specifically from the male Y chromosome. These Y-STRs provide a weaker analysis than autosomal STRs because the Y chromosome is only found in males, which are only passed down by the father, making the Y chromosome in any paternal line practically identical. This causes a significantly smaller amount of distinction between Y ...

  5. Anticipation (genetics) - Wikipedia

    en.wikipedia.org/wiki/Anticipation_(genetics)

    Autosomal dominant. Several spinocerebellar ataxias; Huntington's disease – CAG; Myotonic dystrophy – CTG; Dyskeratosis congenita – TTAGGG (telomere repeat sequence) [1] Autosomal recessive. Friedreich ataxia – GAA (Note: Friedreich ataxia does not usually exhibit anticipation because it is an autosomal recessive disorder. [2]) X-linked

  6. Achondroplasia - Wikipedia

    en.wikipedia.org/wiki/Achondroplasia

    Achondroplasia is a genetic disorder with an autosomal dominant pattern of inheritance whose primary feature is dwarfism. [3] It is the most common cause of dwarfism [4] and affects about 1 in 27,500 people. [3] In those with the condition, the arms and legs are short, while the torso is typically of normal length. [3]

  7. Pseudoautosomal region - Wikipedia

    en.wikipedia.org/wiki/Pseudoautosomal_region

    Crossing over between the X and Y chromosomes is normally restricted to the pseudoautosomal regions; thus, pseudoautosomal genes exhibit an autosomal, rather than sex-linked, pattern of inheritance. So, females can inherit an allele originally present on the Y chromosome of their father.

  8. Introduction to genetics - Wikipedia

    en.wikipedia.org/wiki/Introduction_to_genetics

    Genetics is the study of genes and tries to explain what they are and how they work. Genes are how living organisms inherit features or traits from their ancestors; for example, children usually look like their parents because they have inherited their parents' genes.

  9. Leukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Leukodystrophy

    Inherited forms of leukodystrophy are usually the result of an autosomal recessive inheritance pattern, although dominant inheritance patterns are not unheard of, as in the case of adult-onset leukodystrophy. [14] This means that the affected allele is carried on an autosomal, or non-sex, chromosome and is masked by the dominant, unaffected ...