Mendelian disorders in humans
Mendelian disorders in humans : NEET MCQ Questions
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Contents
- Q 1 : The mode of inheritance for the trait – Fragile X syndrome is________.
- Q 2 : Which of the following is a trait of X-linked recessive?
- Q 3 : Alpha 1 anti-trypsin deficiency is an autosomal recessive genetic disorder. What are the chances that any of the offspring do not express the disease phenotype if both parents are genotype (Aa)?
- Q 4 : Cystic fibrosis is an autosomal recessive genetic disorder. What are the chances that the child would have the disease if any one of the parent (either mother or father)is a carrier of the faulty cystic fibrosis gene (Cc)?
- Q 5 : What will be the condition of the progeny if the father is normal, while the mother has one gene for haemophilia and one gene for colour blindness on one of the X chromosomes?
- Q 6 : If the father in a family has a disease while the mother is normal, the daughters only are inherited by this disease and not the sons. Name this type of disease?
- Q 7 : Which of the following disorder is an example of point mutation?
- Q 8 : Which of the following disorder is also called the Royal disease?
- Q 9 : Which of the following is a type of autosomal recessive genetic disorder?
Question 1 : The mode of inheritance for the trait – Fragile X syndrome is________.
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Question 2 : Which of the following is a trait of X-linked recessive?
Question 3 : Alpha 1 anti-trypsin deficiency is an autosomal recessive genetic disorder. What are the chances that any of the offspring do not express the disease phenotype if both parents are genotype (Aa)?
Question 4 : Cystic fibrosis is an autosomal recessive genetic disorder. What are the chances that the child would have the disease if any one of the parent (either mother or father)is a carrier of the faulty cystic fibrosis gene (Cc)?
Question 5 : What will be the condition of the progeny if the father is normal, while the mother has one gene for haemophilia and one gene for colour blindness on one of the X chromosomes?
Question 6 : If the father in a family has a disease while the mother is normal, the daughters only are inherited by this disease and not the sons. Name this type of disease?
Question 7 : Which of the following disorder is an example of point mutation?
Question 8 : Which of the following disorder is also called the Royal disease?
Question 9 : Which of the following is a type of autosomal recessive genetic disorder?
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