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Genetic Disorders

Total questions: 10

Worksheet time: 6mins

Name
Class
Date
1.

What type of disorder is hemophilia?

a)

Infectious disorder - can get it if you come in contact with someone's blood

b)

Chromosomal disorder - nondisjunction causes this disease due to a missing chromosome

c)

Genetic disorder - inherited from parent(s))

d)

Autoimmune disorder - it develops during your lifetime

2.

Which chromosome is affected in color blindness?

a)

Y chromosome

b)

Z chromosome

c)

X chromosome

d)

W chromosome

3.

What is the main symptom of cystic fibrosis?

a)

Fever

b)

Joint pain

c)

Weight gain

d)

Production of thick, sticky mucus in the airways

4.

What causes Huntington's disease?

a)

Dominant autosomal Gene

b)

Recessive autosomal gene

c)

Lack of physical exercise

d)

Viral infection

5.

How does a child inherit Tay Sachs?

a)

Both parents are carriers

b)

One parent has it and passes it down

c)

Chromosomal mutations

d)

Mom is a carrier dad does not have the gene

6.

Is hemophilia an autosomal or sex-linked disorder?

a)

autosomal

b)

genetic

c)

inherited

d)

sex-linked

7.

Is color blindness more common in males or females?

a)

it is equally common in males and females

b)

both males and females

c)

females

d)

males

8.

Match the disorder types of inheritance

a)

Autosomal Dominant

1.

Huntington's

Dwarfism

b)

Autsomal Recessive

2.

Cystic Fibrosis

Tay Sachs

PKU

c)

Sex-linked

3.

Hemophilia

Color Blindness

Muscular Dyst.

d)

Chromosomal Mutations

4.

Down's Syndrome

Turner

Klinefelter

9.

A mother has Huntington's Disease while the father is normal. What is the possibility her daughter will have it?

a)

25%

b)

0%

c)

75%

d)

50%

10.

A mother is color blind and the husband is normal. What are the chances the son will inherit colorblindness?

a)

0%

b)

100%

c)

25%

d)

50%