Question

	Column-I Name		Column-II(Enzyme)		Column-II (Function)
(A)	Sickle cell anemi	(i)	Due to PP recessive gender	(P)	Valine is arranged in planed of glutamic
(B)	Phenyl ketonuria	(ii)	Homogenetisic acid, Oxidase enzyme is not produced	(Q)	In born error of metabolism
(C)	Alkaptonuria	(iii)	Disease following Mendelian principle	(R)	Urine turns black when comes in contact with air
(D)	Thalassemia	(iv)	Due to homozygous recessive genes	(S)	Haemoglobin is not formed in quantity in blood

Select proper piton from column-I, II and III:–

• A. (A-ii-S)(B-iii-R)(C-i-Q)(D-iv-P)
• B. (A-iv-P)(B-iii-R)(C-i-S)(D-ii-R)
  
• C. (A-iv-P)(B-i-Q)(C-ii-R)(D-iii-S)
• D. (A-iii-R)(B-i-S)(C-iv-P)(D-ii-S)

Answer 1

The correct option is C (A-iv-P)(B-i-Q)(C-ii-R)(D-iii-S)

Sickle cell anemia is one of a group of disorders known as sickle cell disease. Sickle cell anemia is an inherited red blood cell disorder in which there aren't enough healthy red blood cells to carry oxygen throughout your body.

Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine (Phe) metabolism resulting from deficiency of phenylalanine hydroxylase (PAH).

Alkaptonuria is a rare genetic metabolic disorder characterized by the accumulation of homogentisic acid in the body. Affected individuals lack enough functional levels of an enzyme required to breakdown homogentisic acid.

Thalassemia is an inherited blood disorder that causes your
body to have less hemoglobin than normal.

So, the correct answer is "option C"