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  2. X-linked dominant inheritance - Wikipedia

    en.wikipedia.org/wiki/X-linked_dominant_inheritance

    The difference between dominant and recessive inheritance patterns also plays a role in determining the chances of a child inheriting an X-linked disorder from their parentage. [citation needed] X-linked dominant disorders tend to affect females more often because they tend to be developmentally fatal in males.

  3. Bazex–Dupré–Christol syndrome - Wikipedia

    en.wikipedia.org/wiki/Bazex–Dupré–Christol...

    The difference between dominant and recessive inheritance patterns also plays a role in determining the chances of a child inheriting an X-linked disorder from their parentage. [citation needed] A locus of Xq24-q27 has been described. [3]

  4. Sex linkage - Wikipedia

    en.wikipedia.org/wiki/Sex_linkage

    There are fewer X-linked dominant conditions than X-linked recessive, because dominance in X-linkage requires the condition to present in females with only a fraction of the reduction in gene expression of autosomal dominance, since roughly half (or as many as 90% in some cases) of a particular parent's X chromosomes are inactivated in females.

  5. 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.

  6. X-linked hypophosphatemia - Wikipedia

    en.wikipedia.org/wiki/X-linked_hypophosphatemia

    The disorder is inherited in an X-linked dominant manner. [ 1 ] [ 2 ] This means the defective gene responsible for the disorder (PHEX) is located on the X chromosome, and only one copy of the defective gene is sufficient to cause the disorder when inherited from a parent who has the disorder.

  7. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    Autosomal recessive inheritance, a 25% chance, and (purple) a 50% carrier chance. Autosomal recessive traits is one pattern of inheritance for a trait, disease, or disorder to be passed on through families. For a recessive trait or disease to be displayed two copies of the trait or disorder needs to be presented.

  8. X-linked genetic disease - Wikipedia

    en.wikipedia.org/wiki/X-linked_genetic_disease

    X-linked genetic disorders can arise when there is a spontaneous and permanent change in the DNA sequence of an X-linked gene, known as mutation. Traits or diseases caused by X chromosome genes follow X-linked inheritance, the difference between recessive and dominant inheritance affects the probability of an offspring acquiring it from the ...

  9. Simple Mendelian genetics in humans - Wikipedia

    en.wikipedia.org/wiki/Simple_Mendelian_genetics...

    According to the model of Mendelian inheritance, alleles may be dominant or recessive, one allele is inherited from each parent, and only those who inherit a recessive allele from each parent exhibit the recessive phenotype. Offspring with either one or two copies of the dominant allele will display the dominant phenotype.