Genetic Disorders Quest

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Genetic disorders quiz

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alia

United Arab Emirates

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Froggy Jumps Genetic Disorders QuestOnline version Genetic disorders quiz by alia 1 What is the inheritance pattern of cystic fibrosis? a X-linked dominant b Autosomal dominant c Autosomal recessive 2 Which gene is mutated in Huntington's disease? a HTT b BRCA1 c CFTR 3 Down syndrome is most commonly caused by the presence of an extra copy of which chromosome? a Chromosome 21 b Chromosome 18 c Chromosome X 4 Marfan syndrome primarily affects which body system? a Skeletal and cardiovascular systems b Endocrine and nervous systems c Respiratory and digestive systems 5 Which disorder is characterized by a deficiency in the enzyme phenylalanine hydroxylase? a Tay-Sachs disease b Spinal muscular atrophy c Phenylketonuria (PKU) 6 Hemophilia A is caused by a deficiency of which coagulation factor? a Factor IX b Factor VII c Factor VIII 7 Sickle cell disease is due to a mutation in which gene? a CFTR b HBB c HBA1 8 Which chromosomal abnormality is associated with Turner syndrome? a Trisomy 21 b Monosomy X (45,X) c Trisomy 18 9 Which disorder is an example of an autosomal dominant neuromuscular disease? a Myotonic dystrophy b Hemophilia B c Cystic fibrosis 10 Which condition results from a trinucleotide repeat expansion affecting the FMR1 gene? a Prader-Willi syndrome b Fragile X syndrome c Fragile X-associated tremor/ataxia

Froggy Jumps

Genetic Disorders QuestOnline version

Genetic disorders quiz

by alia

What is the inheritance pattern of cystic fibrosis?

X-linked dominant

Autosomal dominant

Autosomal recessive

Which gene is mutated in Huntington's disease?

HTT

BRCA1

CFTR

Down syndrome is most commonly caused by the presence of an extra copy of which chromosome?

Chromosome 21

Chromosome 18

Chromosome X

Marfan syndrome primarily affects which body system?

Skeletal and cardiovascular systems

Endocrine and nervous systems

Respiratory and digestive systems

Which disorder is characterized by a deficiency in the enzyme phenylalanine hydroxylase?

Tay-Sachs disease

Spinal muscular atrophy

Phenylketonuria (PKU)

Hemophilia A is caused by a deficiency of which coagulation factor?

Factor IX

Factor VII

Factor VIII

Sickle cell disease is due to a mutation in which gene?

CFTR

HBB

HBA1

Which chromosomal abnormality is associated with Turner syndrome?

Trisomy 21

Monosomy X (45,X)

Trisomy 18

Which disorder is an example of an autosomal dominant neuromuscular disease?

Myotonic dystrophy

Hemophilia B

Cystic fibrosis

Which condition results from a trinucleotide repeat expansion affecting the FMR1 gene?

Prader-Willi syndrome

Fragile X syndrome

Fragile X-associated tremor/ataxia

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Genetic Disorders Quest

Froggy Jumps

About this activity

Created by

Download the paper version to play

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Genetic Disorders QuestOnline version

by alia

What is the inheritance pattern of cystic fibrosis?

Which gene is mutated in Huntington's disease?

Down syndrome is most commonly caused by the presence of an extra copy of which chromosome?

Marfan syndrome primarily affects which body system?

Which disorder is characterized by a deficiency in the enzyme phenylalanine hydroxylase?

Hemophilia A is caused by a deficiency of which coagulation factor?

Sickle cell disease is due to a mutation in which gene?

Which chromosomal abnormality is associated with Turner syndrome?

Which disorder is an example of an autosomal dominant neuromuscular disease?

Which condition results from a trinucleotide repeat expansion affecting the FMR1 gene?

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