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  2. List of diseases (X) - Wikipedia

    en.wikipedia.org/wiki/List_of_diseases_(X)

    This is a list of diseases starting with the letter "X". X. X, disease; X chromosome, duplication Xq13 1 q21 1; X chromosome, monosomy Xp22 pter ... X chromosome ...

  3. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.

  4. X-linked recessive inheritance - Wikipedia

    en.wikipedia.org/wiki/X-linked_recessive_inheritance

    X-linked recessive inheritance. X-linked recessive inheritance is a mode of inheritance in which a mutation in a gene on the X chromosome causes the phenotype to be always expressed in males (who are necessarily hemizygous for the gene mutation because they have one X and one Y chromosome) and in females who are homozygous for the gene mutation (see zygosity).

  5. X chromosome - Wikipedia

    en.wikipedia.org/wiki/X_chromosome

    If the X chromosome has a genetic disease gene, it always causes illness in male patients, since men have only one X chromosome and therefore only one copy of each gene. Females, instead, require both X chromosomes to have the illness, and as a result could potentially only be a carrier of genetic illness, since their second X chromosome ...

  6. X-linked dominant inheritance - Wikipedia

    en.wikipedia.org/wiki/X-linked_dominant_inheritance

    X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome. As an inheritance pattern, it is less common than the X-linked recessive type.

  7. Category:Genes on human chromosome X - Wikipedia

    en.wikipedia.org/wiki/Category:Genes_on_human...

    Complete list of genes on human chromosome X; CCDS: Gene list: HGNC: Gene list: UniProt: Gene list: ... ZC4H2-Associated Rare Disorders; 0–9. 40S ribosomal protein ...

  8. What is ‘Disease X’ and why are experts worried? - AOL

    www.aol.com/disease-x-why-experts-worried...

    “This concept [of Disease X] was one of the lessons we learned from this pandemic,” Dr Russo said. “As mankind breaks down these barriers [between humans and other species] through live ...

  9. Sex chromosome anomalies - Wikipedia

    en.wikipedia.org/wiki/Sex_chromosome_anomalies

    Sex chromosome anomalies belong to a group of genetic conditions that are caused or affected by the loss, damage or addition of one or both sex chromosomes (also called gonosomes). In humans this may refer to: 45, X, also known as Turner syndrome; 45,X/46,XY mosaicism, also known as X0/XY mosaicism and mixed gonadal dysgenesis; 46, XX/XY

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