In which of the following one may observe variation in DNA?

1. Fragmentation

2. Budding

3. Amitosis

4. mutation

Subtopic:  Mendelian Disorders |
 95%
Level 1: 80%+
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Mendelian disorders are mainly determined by:
1. Alteration or mutation in a single gene.
2. Chromosomal gross structural changes.
3. Recombination between linked genes.
4. Jumping genes

Subtopic:  Mendelian Disorders |
 82%
Level 1: 80%+
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Cystic fibrosis, Myotonic dystrophy and Thalassemia are

1. Chromosomal disorders

2. Autosomal recessive disorders

3. Mendelian disorders

4. Autosomal dominant disorders

Subtopic:  Mendelian Disorders |
 65%
Level 2: 60%+
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Which of the following is not a hereditary disease?

1. Haemophilia. 

2. Cretinism. 

3. Cystic fibrosis. 

4. Thalassemia.

Subtopic:  Mendelian Disorders |
 84%
Level 1: 80%+
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Two phenotypically normal individuals have an affected child. What can we conclude about the parents?

1. they both carried the diesease allele

2. they are not the parents of the child

3. they are affected

4. no conclusions can be drawn

Subtopic:  Mendelian Disorders |
 91%
Level 1: 80%+
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Which one of the following traits are controlled by genes located on the differential part of X-chromosome?

1. Porcupine skin and epidermolysis bullosa

2. Beard in man and milk glands in female

3. Color blindness and hemophilia

4. Color blindness and cystic fibrosis

Subtopic:  Mendelian Disorders |
 88%
Level 1: 80%+
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How many diseases in the list given below are Mendelian disorders?

1.  Four

2.  Five

3.  Six

4.  Seven 

Subtopic:  Mendelian Disorders |
 83%
Level 1: 80%+
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Which of the following occurs due to the presence of autosome linked dominant trait?

1. Thalessemia 2. Sickle cell anaemia
3. Myotonic dystrophy 4. Haemophilia
Subtopic:  Mendelian Disorders |
 82%
Level 1: 80%+
NEET - 2022

Sorry!! currently, the explanation for the question is not provided. If you need further help, please email at support@neetprep.com with subject: Explanation Missing for Question Id: 339461

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Sorry!! currently, the explanation for the question is not provided. If you need further help, please email at support@neetprep.com with subject: Explanation Missing for Question Id: 339461


Which of the following is NOT an autosomal recessive disorder? 
1. Sickle cell anemia 
2. Phenylketonuria 
3. Haemophilia
4. Thalassemia
Subtopic:  Mendelian Disorders | Mendelian Disorders: Hemophilia |
 79%
Level 2: 60%+
NEET - 2024

Sorry!! currently, the explanation for the question is not provided. If you need further help, please email at support@neetprep.com with subject: Explanation Missing for Question Id: 456753

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Sorry!! currently, the explanation for the question is not provided. If you need further help, please email at support@neetprep.com with subject: Explanation Missing for Question Id: 456753


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In Phenylketonuria,

I: Phenylpyruvic acid and other derivatives are accumulated in brain resulting in mental retardation.
II: These are also excreted through urine because of its poor absorption by kidney.


1. Only I is correct
2. Only II is correct
3. Both are correct
4. Both are incorrect

Subtopic:  Mendelian Disorders |
 88%
Level 1: 80%+
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