Genetic Disorders

Genetic Disorders

9th - 12th Grade

20 Qs

quiz-placeholder

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Genetic Disorders

Genetic Disorders

Assessment

Quiz

Biology

9th - 12th Grade

Medium

NGSS
HS-LS3-1, HS-LS3-2, HS-LS3-3

+1

Standards-aligned

Created by

Chidi Iromuanya

Used 341+ times

FREE Resource

20 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

5 mins • 1 pt

Media Image

Study the blood cells in the picture below. Describe the genotype for the individual with these types of cells.

homozygous recessive

heterozygous

homozygous dominant

codominant

Tags

NGSS.HS-LS3-1

NGSS.HS-LS3-2

2.

MULTIPLE CHOICE QUESTION

5 mins • 1 pt

Which disorder is treated by restricting milk in the diet?

phenylketonuria

cystic fibrosis

galactosemia

Tay-Sachs disease

3.

MULTIPLE CHOICE QUESTION

5 mins • 1 pt

Down syndrome is the result of an extra chromosome 21 in a gamete. What caused this to happen?

nondisjunction

telomeres

environment

chromosome inactivation

4.

MULTIPLE CHOICE QUESTION

5 mins • 1 pt

Why is Down syndrome called trisomy 21

The person has 21 pairs of chromosomes instead of 23.

The person has an abnormal gene on chromosome 21.

The syndrome is caused by having 21 pairs of autosomes.

The syndrome results from an extra chromosome 21.

5.

MULTIPLE CHOICE QUESTION

5 mins • 1 pt

What is the effect of sickle-cell anemia?

blocked respiratory pathways

decreased neurological functions

inefficient oxygen transportation

susceptibility to contracting malaria

6.

MULTIPLE CHOICE QUESTION

5 mins • 1 pt

You and your colleagues are constructing a pedigree for a boy with cystic fibrosis. The individual’s younger brother has also been diagnosed with cystic fibrosis. How would these brothers be represented in a pedigree?

Both would be represented as completely shaded circles.

Both would be represented as completely shaded squares.

The older brother would be a shaded square, while the younger brother would be a half-shaded square.

Both would be represented as unshaded squares.

Tags

NGSS.HS-LS3-1

NGSS.HS-LS3-2

7.

MULTIPLE CHOICE QUESTION

5 mins • 1 pt

A man carrying the allele for Huntington’s disease marries a woman who is homozygous recessive for the allele. What is the probability that their offspring will develop Huntington’s disease?

25 percent

50 percent

75 percent

100 percent

Tags

NGSS.HS-LS3-1

NGSS.HS-LS3-2

NGSS.HS-LS3-3

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