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Given below is a pedigree analysis of one unknown disease in human. Which of the following is the best explanation?

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Important Questions on Heredity and Variation

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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
A human female with Turner's syndrome
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
A disease caused by an autosomal primary non-disjunction is
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
Which of the following muscular disorders is inherited?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
Select the correct match.
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
Which of the following most appropriately describes haemophilia?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
Conditions of a karyotype 2n±1 and 2n±2 are called
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
The genetic disorder in which an individual has an overall masculine development, gynaecomastia and is sterile:
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
A change of single base pair in the gene for beta globin chain (in human haemoglobin) that results in the change of amino acid residue glutamine to valine which is due to
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
If a colour-blind man marries a woman who is homozygous for normal colour vision, the probability of their son being colour-blind is
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
A couple has two sons and two daughters. Only one son is colour blind and the rest of the siblings are normal. Assuming colour blindness is sex-linked, which ONE of the following would be the phenotype of the parents?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
In the following human pedigree, the filled symbols represents the affected individuals. Identify the type of given pedigree.


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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
Pick out the correct statements:
(i) Haemophilia is a sex-linked recessive disease.
(ii) Down's syndrome is due to aneuploidy.
(iii) Phenylketonuria is an autosomal recessive gene disorder.
(iv) Sickle cell anaemia is an X-linked recessive gene disorder.
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
Point mutation is caused in which of the following diseases?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
A man whose father was colour blind marries a woman who had a colour blind mother and normal father. What percentage of male children of this couple will be colour blind?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
In an Organism, mutation in a single gene exhibits multiple phenotypic expression. Identify the underlying genetic mechanism in the above instance.
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
Which one of the following conditions is not responsible for the presence of deoxygenated blood in the arteries of a newborn?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans

Statement (S): The heterozygous individuals for sickle-cell anaemia HbAHbS express disease phenotype and also carriers of the disease.

Reason (R): HbAHbS genotype individuals are resistant to severe effects of malaria.

The correct answer is

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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
Thalassemia and sickle cell anaemia are caused due to a problem in globin molecule synthesis. Select the correct statement.
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
An abnormal human baby with 'XXX' sex chromosomes was born due to:
HARD
Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorders in Humans
A colourblind man marries a woman with normal sight who has no history of colour blindness in her family. What is the probability of their sons being colourblind?