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Glossary

Definitions for terms commonly found on our site

  • Allele
    One of several alternative forms of a gene sequence at a specific Locus.
  • Alopecia
    A condition where some or all hair is lost from the head and/or other parts of the body.
  • Amino Acid
    Organic compounds that combine to form proteins.
  • Anemia
    Decrease in the number of red blood cells (RBCs) or less than the normal quantity of hemoglobin in the blood.
  • Ataxia
    The loss of voluntary coordinated movement of the body, indicating an underlying neurologic issue.
  • Atrophy
    The partial or complete wasting away of a part of the body, such as the muscles.
  • Autosomal Dominant
    A pattern of inheritance where an affected dog has one copy of a gene with a mutation and one normal gene. Offspring have a 50% chance of inheriting the disease-causing gene.
  • Autosomal Recessive
    A pattern of inheritance in which an affected dog must have two copies of an abnormal gene to present with the disease or trait.
  • Cardiovascular
    A broad category of diseases that affect the heart and/or blood vessels.
  • Carrier
    A dog that has only one copy of an abnormal gene for a recessive disease. Carriers do not typically show disease symptoms but can pass on the gene to 
    offspring.
  • Cataract
    A clouding of the lens inside the eye that leads to decreased vision.
  • Cerebellum
    A structure in the brain known to control voluntary movements of the body.
  • Cerebrospinal Fluid
    Clear fluid in the spinal cord and surrounding the brain that acts as a cushion, protecting the brain and spine from injury.
  • Chromosome
    An organized structure of DNA and protein found in cells, encoding most or all of a dog's genetic information. Dogs have 78 chromosomes (39 pairs).
  • Collagen
    A protein that is the main component of Connective Tissue, including ligaments, tendons, bones, and skin.
  • Coloboma
    A keyhole-shaped defect of the eye present from birth.
  • Cone Cells
    Photoreceptor cells in the Retina responsible for color vision, especially in bright light.
  • Connective Tissue
    A fibrous type of tissue that provides support for other tissues.
  • Cryptorchidism
    Failure of one or both testicles to descend into the scrotum.
  • Dementia
    Progressive cognitive decline, including memory deficits and decreased responsiveness to stimuli.
  • Dominant Modifier
    A gene that alters the expression of another gene, requiring only one copy to influence the trait.
  • Electroretinogram
    An eye test that evaluates the function of Rod and Cone cells in the Retina.
  • Enzyme
    Complex proteins that catalyze chemical reactions in the body.
  • Exon
    The segments of a gene whose sequence is expressed as messenger RNA and usually translated into a protein.
  • Glaucoma
    Increased pressure within the eye.
  • Haplotype
    A series of alleles found at linked loci on a single Chromosome.
  • Hemorrhage
    Excessive bleeding.
  • Heterozygous
    Having two different alleles at a particular Locus.
  • Homozygous
    Having identical alleles at a particular Locus.
  • Hyperparathyroidism
    Over-secretion of the parathyroid hormone from the parathyroid glands.
  • Hypocalcemia
    Insufficient amount of calcium in the blood.
  • Hypoglycemia
    Low blood sugar.
  • Hypomineralization
    Insufficient levels of minerals, typically referring to bones and teeth.
  • Hysterectomy
    Removal of a female dog's uterus.
  • In Utero
    Before birth; in the uterus.
  • Inclusion Bodies
    Aggregates of protein in a cell visible under a microscope.
  • Incomplete Penetrance
    When an individual has a Mutation but does not show signs of the disease.
  • Locus
    The specific site of a gene on a Chromosome.
  • Lysosomal Storage Disorder
    A group of metabolic disorders caused by the absence of a specific Enzyme, leading to abnormal accumulation of substances in the body.
  • Melanin
    A natural pigment that gives color to hair, skin, and the iris of the eye.
  • Metabolic Acidosis
    Occurs when the body produces too much acid or when the kidneys fail to remove enough acid.
  • Mitochondrial Inheritance
    A pattern of inheritance where traits are passed down from the mother through mitochondrial DNA. Male dogs do not pass on mitochondrial diseases.
  • Mitochondrion
    A cell organelle responsible for energy production, containing its own DNA (mtDNA).
  • Mucous Membrane
    A mucus-secreting tissue lining the mouth, nose, genitals, esophagus, and rectum.
  • Multigenic Associative Markers
    Genetic variations in multiple genes associated with a disease or trait but not the direct cause.
  • Musculoskeletal
    A broad category of diseases affecting muscles and/or bones.
  • Mutation
    A change from the normal form of a gene.
  • Myelin
    An insulating layer of protein and fat that surrounds nerves, aiding rapid signal transmission.