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  2. 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.

  3. Category:Genetic animal diseases - Wikipedia

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

    Pages in category "Genetic animal diseases" ... Online Mendelian Inheritance in Animals This page was last edited on 20 September 2016, at 16:41 (UTC). ...

  4. Genetic disorder - Wikipedia

    en.wikipedia.org/wiki/Genetic_disorder

    There are well over 6,000 known genetic disorders, [4] and new genetic disorders are constantly being described in medical literature. [5] More than 600 genetic disorders are treatable. [6] Around 1 in 50 people are affected by a known single-gene disorder, while around 1 in 263 are affected by a chromosomal disorder. [7]

  5. Lists of animal diseases - Wikipedia

    en.wikipedia.org/wiki/Lists_of_animal_diseases

    List of aquarium diseases; List of dog diseases; List of feline diseases; List of diseases of the honey bee; List of diseases spread by invertebrates; Poultry disease; Lists of zoonotic diseases, infectious diseases that have jumped from an animal to a human

  6. Severe combined immunodeficiency (non-human) - Wikipedia

    en.wikipedia.org/wiki/Severe_combined...

    A common cause of death is canine distemper, which develops following vaccination with a modified live distemper virus vaccine. [10] Due to its similarity to X-SCID in humans, breeding colonies of affected dogs have been created in order to study the disease and test treatments, particularly bone marrow transplantation and gene therapy. [11]

  7. Cerebellar abiotrophy - Wikipedia

    en.wikipedia.org/wiki/Cerebellar_abiotrophy

    There are other diseases that lead to cerebellar degeneration, but the loss of Purkinje cells is a clear way to diagnose cerebellar abiotrophy, and the combination of clinical signs is sufficiently unique that cerebellar abiotrophy can easily be distinguished from other conditions, even in a living animal.

  8. Lethal allele - Wikipedia

    en.wikipedia.org/wiki/Lethal_allele

    The heterozygous and homozygous phenotype is still expressed in most cases if two different disease-causing alleles are present. Achondroplasia is a skeletal system disorder caused by a recessive allele that can still result in a live birth in the homozygous state.

  9. Ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Ichthyosis

    Ichthyosis (also named fish scale disease) [1] is a family of genetic skin disorders characterized by dry, thickened, scaly skin. [2] The more than 20 types of ichthyosis range in severity of symptoms, outward appearance, underlying genetic cause and mode of inheritance (e.g., dominant, recessive, autosomal or X-linked). [3]

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