
GENETIC DISEASES A04
Biology
9th Grade
10 Questions
NGSS covered
Used 165+ times

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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Located on chromosome 4, this neurological disorder is caused by the presence of a DOMINANT ALLELE.
dislexia
Hunington Disease
Turner syndrome
Fragile X
Tags
NGSS.HS-LS3-2
NGSS.HS-LS3-1
2.
MULTIPLE CHOICE QUESTION
1 min • 1 pt
This genetic disorder is an example of monosomy, and is characterized by a karyotype of 45XO or 45X. It only affects women.
Phenylketonuria
Anemia
Fragile X
Turner Syndrome
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
This genetic disorder is caused by non-disjunction of the 21st chromosome. It is one of the most common chromosomal disorders.
Turner syndrome
Hunington Disease
Down syndrome
Myopia
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
This genetic disorder causes a reduction/absence of melanin in the skin, hair and eyes. Located on chromosome 6, this disorder is common throughout the animal kingdom.
Anemia
Albinism
Myopia
Hemophilia
Tags
NGSS.HS-LS3-2
5.
MULTIPLE CHOICE QUESTION
1 min • 1 pt
This genetic disorder occurs on chromosome 12. This disorder does not allow for the breakdown of phenylalanine in the diet. Buildup of phenylalanine in the body can cause severe symptoms and even reduce lifespan.
Hunington Disease
Sickle-cell Anemia
Phenylketonuria
Myopia
Tags
NGSS.HS-LS3-2
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
This genetic disorder causes red blood cells to exhibit an irregular shape. Symptoms of this disorder can include joint pain, poor circulation, and a shorter lifespan. It is highly prevalent in African and African American populations.
Anemia
Albinism
Turner syndrome
Sickle-cell Anemia
Tags
NGSS.HS-LS3-2
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Fragile X
causes cognitive impairment
occurs on the X chromosome
causes learning disabilities
all of these are characteristics of Fragile X
Tags
NGSS.HS-LS3-2
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