मराठी

About 8% of the human male population suffers from colour blindness, whereas only about 0.4% of the human female population suffers from this disease. Write an explanation to show how it is possible. - Biology

Advertisements
Advertisements

प्रश्न

About 8% of the human male population suffers from colour blindness, whereas only about 0.4% of the human female population suffers from this disease. Write an explanation to show how it is possible.

लघु उत्तर
Advertisements

उत्तर

Colour blindness is a sex-linked disorder and is caused by a recessive gene located on the X chromosome. The Y chromosome of male does not carry any gene for colour vision and the defect appears in the presence of a single recessive gene (XcY). As a result, colour blindness is more common in males (8%) as compared to females (0.4%).

shaalaa.com
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 5: Principles of Inheritance and Variation - HIGHER ORDER THINKING SKILLS QUESTIONS [पृष्ठ २१०]

APPEARS IN

नूतन Biology [English] Class 12 ISC
पाठ 5 Principles of Inheritance and Variation
HIGHER ORDER THINKING SKILLS QUESTIONS | Q 24. | पृष्ठ २१०

संबंधित प्रश्‍न

What are the different characters that develop due to Klinefelter's syndrome?


Give an account of one Mendelian and one chromosomal disorder you have studied.


Read the following statements and select the correct option.

i. Genetic disorders are broadly categorised as, Mendelian disorders and chromosomal disorders.

ii. Mendelian disorders are caused due to absence or excess of one or more chromosomes or their abnormal arrangement.

iii. Chromosomal disorders are mainly caused due to alteration or mutation in the gene.


Identify the INCORRECT statement.


Following list indicates various genetic diseases. Identify the diseases that are not caused due to single gene defect.

Huntington's chorea, alkaptonuria, Sickle cell anaemia, Down syndrome, thalassemia, Taysachs disease, Turner syndrome, cystic fibrosis, haemophi Lia, Klinefelter syndrome, albinism


The most striking example of point mutation is found in a disease called ______.


This abnormality occurs due to monosomy (2n - 1); the individual has 2n = 45 chromosomes with 44 + XO genotype.


Females with Turner’s syndrome have ______.


Read the following and answer from given below:

According to Mendel, one gene controls the expression of one character only. The ability of a gene to have multiple phenotypic effects because it influences a number of characters are an exception. The gene has multiple phenotypic effects because its ability to control two or more characters can be seen in cotton. In cotton, a gene for the lint also influences the height of the plant, size of the ball, number of ovules, and viability of seeds.

Which of the following disorder is an example of genes with multiple phenotypic effects?


The practice of analyzing inheritance patterns in human beings is called ______


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×