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BIOETHICS ชีววิทยากับอาชีพที่หลากหลาย - Coggle Diagram

- - - - Heredity or characteristics in living things can be passed on to the next generation by through the germ cells
    - - Persistent genetic variation
        
        It is a genetic trait that cannot be distinguished clearly such as height, weight, skeletal structure, and skin color.
      - Discrete genetic variation
        
        For example: dimples - no dimples, right dizzy - left dizzy, can wrap tongue - can't wrap tongue, earlobes - don't have earlobes, thumb bone can sway - can't budge
  - - - A condition in which the kidneys are working less or less. The function of the kidneys is to eliminate waste and toxins. out of the body Hormone secretion Regulating water and minerals in the body when the kidneys are less active, they can't get rid of waste or toxins from the body
    - - is a hereditary disease of red blood cells. Normally, red blood cells are circular in shape. This results in red blood cells being flexible so they can travel through the smallest blood vessels.
    - - Diseases with airway narrowing become more and more common as the disease progresses, typically including chronic bronchitis and emphysema. As a result, breathing for oxygen exchange is not good.
    - - genetic disease It is caused by a mutation in the Huntington gene, one of two genes in the body. This is a trinucleotide repeat of the CAG (trinucleotide repeat) base.
    - - a type of anemia caused by abnormal blood cells This causes red blood cells to be short-lived, brittle, ruptured, easily destroyed and inherited through recessive genes. Caused by abnormalities in genes that control hemoglobin, an important substance in red blood cells.
    - - Hereditary bleeding disorders which makes the blood unable to clot This leads to severe, uncontrolled bleeding that can lead to disability or death. Spontaneous bleeding or after minor injuries When the patient has symptoms of bleeding will
    - - Down syndrome is a chromosomal disorder. and is a genetic disease caused by the presence of chromosome 21 in whole or in part. which most patients will have delayed development