Which disease is caused by a gene defect located on chromosome $16$,leading to a deficiency that affects the transport of respiratory gases?

  • A
    Hemophilia
  • B
    Sickle cell anemia
  • C
    $\alpha$-Thalassemia
  • D
    $\beta$-Thalassemia

Explore More

Similar Questions

If both the mother and father are without pigments (albinism),then:

Assertion: Phenylketonuria is an autosomal recessive hereditary disease caused by the body's failure to oxidize the amino acid $phenylalanine$ to $tyrosine$ due to a defective enzyme.
Reason: It results in the accumulation of $phenylpyruvic$ acid and its derivatives in the urine.

In the following human pedigree,the filled symbols represent the affected individuals. Identify the type of given pedigree.

$A$: The heterozygotic female for haemophilia may transmit the disease to sons.
$R$: Such traits show criss-cross inheritance.

Disorders inherited according to Mendel's laws of inheritance are called:

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo