How do genetic disorders arise? Explain by giving suitable examples.

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(N/A) Every feature in an organism is controlled by one or more genes located on the $DNA$ present in the chromosomes. $DNA$ is the carrier of genetic information and is typically transmitted from one generation to the next without any change.
However,alterations or changes in the genetic material can occur,which are referred to as mutations. $A$ number of disorders in human beings are associated with the inheritance of these altered genes or chromosomes.
Genetic disorders are broadly classified into two categories:
$1$. Mendelian Disorders: These are primarily determined by alteration or mutation in a single gene. Examples include Haemophilia,Cystic fibrosis,Colour blindness,Sickle cell anaemia,Thalassemia,and Phenylketonuria.
$2$. Chromosomal Disorders: These are caused by an excess,absence,or abnormal arrangement of one or more chromosomes. Examples include Down's syndrome,Turner's syndrome,and Klinefelter's syndrome.

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Similar Questions

Genes that are similar in phenotypic effect when present separately,but together interact to produce a different trait and the ratio is $9:7$ in the $F_2$ generation. What are such genes known as?

Select the incorrect statement:

The phenotype of an organism is the result of?

Why does a new organism differ from its parents in its characteristics?

Match List-$I$ with List-$II$ :
List-$I$ (Type of Inheritance) List-$II$ (Example)
$A$. Incomplete dominance $I$. Blood groups in human
$B$. Co-dominance $II$. Flower colour in Antirrhinum
$C$. Pleiotropy $III$. Skin colour in human
$D$. Polygenic inheritance $IV$. Phenylketonuria

Choose the correct answer from the options given below :

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