02bb_f873
Which one of the following genetic disorders correspond to the description 'a condition that affects only females, results when one of their X chromosomes is missing or partially missing'.
A. Beta-Thalassemia Incorrect B. DiGeorge syndrome Incorrect C. Phenylketonuria Incorrect D. Philadelphia chromosome Incorrect E. Turner syndrome Correct MC02bb_fb93
Which one of the following genetic disorders correspond to the description 'a condition that affects only females, results when one of their X chromosomes is missing or partially missing'.
A. Angelman syndrome Incorrect B. Cystic fibrosis Incorrect C. Galactosemia Incorrect D. Patau syndrome Incorrect E. Turner syndrome Correct MC0cb7_74cb
Which one of the following genetic disorders correspond to the description 'gets its name from the distinctive sweet odor of affected infants' urine'.
A. Cystic fibrosis Incorrect B. Maple syrup urine disease Correct C. Sickle-cell anemia Incorrect D. Turner syndrome Incorrect E. WAGR syndrome Incorrect MC0cb7_a775
Which one of the following genetic disorders correspond to the description 'gets its name from the distinctive sweet odor of affected infants' urine'.
A. Angelman syndrome Incorrect B. Edwards syndrome Incorrect C. Hemophilia Incorrect D. Maple syrup urine disease Correct E. Turner syndrome Incorrect MC0d58_0d3c
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 22 is missing'.
A. DiGeorge syndrome Correct B. Down syndrome Incorrect C. Duchenne muscular dystrophy Incorrect D. Klinefelter syndrome Incorrect E. Marfan syndrome Incorrect MC0d58_2b6a
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 22 is missing'.
A. DiGeorge syndrome Correct B. Patau syndrome Incorrect C. Prader-Willi syndrome Incorrect D. Tay-Sachs disease Incorrect E. Triple X syndrome Incorrect MC1049_2977
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 11 is missing'.
A. Cri du chat syndrome Incorrect B. Down syndrome Incorrect C. Patau syndrome Incorrect D. Philadelphia chromosome Incorrect E. WAGR syndrome Correct MC1049_f6f9
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 11 is missing'.
A. Galactosemia Incorrect B. Maple syrup urine disease Incorrect C. Prader-Willi syndrome Incorrect D. WAGR syndrome Correct E. Wolf-Hirschhorn syndrome Incorrect MC135b_7a60
Which one of the following genetic disorders correspond to the description 'genetic disorder caused by the presence of all or part of a third copy of chromosome 13'.
A. Hemophilia Incorrect B. Patau syndrome Correct C. Tay-Sachs disease Incorrect D. WAGR syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MC135b_8e72
Which one of the following genetic disorders correspond to the description 'genetic disorder caused by the presence of all or part of a third copy of chromosome 13'.
A. Achondroplasia Incorrect B. Angelman syndrome Incorrect C. Patau syndrome Correct D. Turner syndrome Incorrect E. WAGR syndrome Incorrect MC1411_7238
Which one of the following genetic disorders correspond to the description 'disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain'.
A. Cystic fibrosis Incorrect B. DiGeorge syndrome Incorrect C. Duchenne muscular dystrophy Incorrect D. Edwards syndrome Incorrect E. Huntington's disease Correct MC1411_de4c
Which one of the following genetic disorders correspond to the description 'disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain'.
A. Angelman syndrome Incorrect B. DiGeorge syndrome Incorrect C. Duchenne muscular dystrophy Incorrect D. Huntington's disease Correct E. Klinefelter syndrome Incorrect MC1a8e_41f2
Which one of the following genetic disorders correspond to the description 'caused by a deletion within HSA band on the short arm of chromosome 4'.
A. Cystic fibrosis Incorrect B. Duchenne muscular dystrophy Incorrect C. Fragile X syndrome Incorrect D. Klinefelter syndrome Incorrect E. Wolf-Hirschhorn syndrome Correct MC1a8e_7250
Which one of the following genetic disorders correspond to the description 'caused by a deletion within HSA band on the short arm of chromosome 4'.
A. Down syndrome Incorrect B. Hemophilia Incorrect C. Huntington's disease Incorrect D. Maple syrup urine disease Incorrect E. Wolf-Hirschhorn syndrome Correct MC1a8e_774a
Which one of the following genetic disorders correspond to the description 'caused by a deletion within HSA band on the short arm of chromosome 4'.
A. Cri du chat syndrome Incorrect B. DiGeorge syndrome Incorrect C. Fragile X syndrome Incorrect D. Turner syndrome Incorrect E. Wolf-Hirschhorn syndrome Correct MC1a8e_a1b9
Which one of the following genetic disorders correspond to the description 'caused by a deletion within HSA band on the short arm of chromosome 4'.
A. Cri du chat syndrome Incorrect B. Marfan syndrome Incorrect C. Phenylketonuria Incorrect D. Triple X syndrome Incorrect E. Wolf-Hirschhorn syndrome Correct MC34f9_9b8b
Which one of the following genetic disorders correspond to the description 'individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes'.
A. Beta-Thalassemia Incorrect B. DiGeorge syndrome Incorrect C. Maple syrup urine disease Incorrect D. Marfan syndrome Correct E. Prader-Willi syndrome Incorrect MC34f9_e055
Which one of the following genetic disorders correspond to the description 'individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes'.
A. Angelman syndrome Incorrect B. Duchenne muscular dystrophy Incorrect C. Marfan syndrome Correct D. Tay-Sachs disease Incorrect E. Wolf-Hirschhorn syndrome Incorrect MC34f9_fa92
Which one of the following genetic disorders correspond to the description 'individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes'.
A. Angelman syndrome Incorrect B. Beta-Thalassemia Incorrect C. Hemophilia Incorrect D. Marfan syndrome Correct E. Triple X syndrome Incorrect MC3b4f_0910
Which one of the following genetic disorders correspond to the description 'a genetic condition involving changes in part of the X chromosome'.
A. DiGeorge syndrome Incorrect B. Edwards syndrome Incorrect C. Fragile X syndrome Correct D. Maple syrup urine disease Incorrect E. Phenylketonuria Incorrect MC3b4f_6303
Which one of the following genetic disorders correspond to the description 'a genetic condition involving changes in part of the X chromosome'.
A. Achondroplasia Incorrect B. Fragile X syndrome Correct C. Phenylketonuria Incorrect D. Sickle-cell anemia Incorrect E. Wolf-Hirschhorn syndrome Incorrect MC53b4_758b
Which one of the following genetic disorders correspond to the description 'impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull'.
A. Achondroplasia Correct B. Beta-Thalassemia Incorrect C. Duchenne muscular dystrophy Incorrect D. Fragile X syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MC53b4_848e
Which one of the following genetic disorders correspond to the description 'impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull'.
A. Achondroplasia Correct B. Angelman syndrome Incorrect C. Patau syndrome Incorrect D. Prader-Willi syndrome Incorrect E. WAGR syndrome Incorrect MC5461_18a1
Which one of the following genetic disorders correspond to the description 'result of a random error that causes a person to be born with an extra chromosome 18'.
A. Cystic fibrosis Incorrect B. DiGeorge syndrome Incorrect C. Edwards syndrome Correct D. Prader-Willi syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MC5461_9e0c
Which one of the following genetic disorders correspond to the description 'result of a random error that causes a person to be born with an extra chromosome 18'.
A. Beta-Thalassemia Incorrect B. Cystic fibrosis Incorrect C. Duchenne muscular dystrophy Incorrect D. Edwards syndrome Correct E. Wolf-Hirschhorn syndrome Incorrect MC5f39_54b5
Which one of the following genetic disorders correspond to the description 'forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material'.
A. Cri du chat syndrome Incorrect B. Duchenne muscular dystrophy Incorrect C. Klinefelter syndrome Incorrect D. Philadelphia chromosome Correct E. Wolf-Hirschhorn syndrome Incorrect MC6075_754e
Which one of the following genetic disorders correspond to the description 'a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat'.
A. Achondroplasia Incorrect B. Cystic fibrosis Correct C. Galactosemia Incorrect D. Maple syrup urine disease Incorrect E. Tay-Sachs disease Incorrect MC6075_e05e
Which one of the following genetic disorders correspond to the description 'a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat'.
A. Cystic fibrosis Correct B. Edwards syndrome Incorrect C. Patau syndrome Incorrect D. Prader-Willi syndrome Incorrect E. WAGR syndrome Incorrect MC61bb_6aa3
Which one of the following genetic disorders correspond to the description 'inherited disorder that causes an amino acid called phenylalanine to build up in the body'.
A. Cri du chat syndrome Incorrect B. DiGeorge syndrome Incorrect C. Phenylketonuria Correct D. WAGR syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MC61bb_81a7
Which one of the following genetic disorders correspond to the description 'inherited disorder that causes an amino acid called phenylalanine to build up in the body'.
A. Angelman syndrome Incorrect B. Cystic fibrosis Incorrect C. Duchenne muscular dystrophy Incorrect D. Marfan syndrome Incorrect E. Phenylketonuria Correct MC61bb_8e2c
Which one of the following genetic disorders correspond to the description 'inherited disorder that causes an amino acid called phenylalanine to build up in the body'.
A. Cystic fibrosis Incorrect B. Down syndrome Incorrect C. Phenylketonuria Correct D. Philadelphia chromosome Incorrect E. Triple X syndrome Incorrect MC61bb_a0a6
Which one of the following genetic disorders correspond to the description 'inherited disorder that causes an amino acid called phenylalanine to build up in the body'.
A. Cystic fibrosis Incorrect B. Fragile X syndrome Incorrect C. Marfan syndrome Incorrect D. Phenylketonuria Correct E. Philadelphia chromosome Incorrect MC6ae4_011f
Which one of the following genetic disorders correspond to the description 'autosomal recessive genetic disorder affecting most critically the lungs'.
A. Cystic fibrosis Correct B. Fragile X syndrome Incorrect C. Galactosemia Incorrect D. Phenylketonuria Incorrect E. Philadelphia chromosome Incorrect MC6ae4_96ad
Which one of the following genetic disorders correspond to the description 'autosomal recessive genetic disorder affecting most critically the lungs'.
A. Cystic fibrosis Correct B. Galactosemia Incorrect C. Sickle-cell anemia Incorrect D. WAGR syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MC6ae4_afc3
Which one of the following genetic disorders correspond to the description 'autosomal recessive genetic disorder affecting most critically the lungs'.
A. Cystic fibrosis Correct B. Duchenne muscular dystrophy Incorrect C. Fragile X syndrome Incorrect D. Hemophilia Incorrect E. Tay-Sachs disease Incorrect MC6ae4_df73
Which one of the following genetic disorders correspond to the description 'autosomal recessive genetic disorder affecting most critically the lungs'.
A. Cri du chat syndrome Incorrect B. Cystic fibrosis Correct C. DiGeorge syndrome Incorrect D. Klinefelter syndrome Incorrect E. Triple X syndrome Incorrect MC6d2d_38b0
Which one of the following genetic disorders correspond to the description 'disorder that is due to a missing piece (deletion) of a specific part of chromosome 11'.
A. Achondroplasia Incorrect B. Cystic fibrosis Incorrect C. Klinefelter syndrome Incorrect D. Tay-Sachs disease Incorrect E. WAGR syndrome Correct MC6d2d_ae1f
Which one of the following genetic disorders correspond to the description 'disorder that is due to a missing piece (deletion) of a specific part of chromosome 11'.
A. Achondroplasia Incorrect B. Angelman syndrome Incorrect C. Marfan syndrome Incorrect D. Tay-Sachs disease Incorrect E. WAGR syndrome Correct MC7054_31e9
Which one of the following genetic disorders correspond to the description 'result of a random error that causes a person to be born with an extra chromosome 21'.
A. Angelman syndrome Incorrect B. Cystic fibrosis Incorrect C. Down syndrome Correct D. Phenylketonuria Incorrect E. Philadelphia chromosome Incorrect MC760d_3cf3
Which one of the following genetic disorders correspond to the description 'a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord'.
A. Cystic fibrosis Incorrect B. Phenylketonuria Incorrect C. Tay-Sachs disease Correct D. WAGR syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MC760d_a6d2
Which one of the following genetic disorders correspond to the description 'a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord'.
A. Angelman syndrome Incorrect B. Patau syndrome Incorrect C. Philadelphia chromosome Incorrect D. Prader-Willi syndrome Incorrect E. Tay-Sachs disease Correct MC766e_5e53
Which one of the following genetic disorders correspond to the description 'metabolic disorder affecting branched-chain amino acids'.
A. Cri du chat syndrome Incorrect B. Galactosemia Incorrect C. Maple syrup urine disease Correct D. Sickle-cell anemia Incorrect E. Triple X syndrome Incorrect MC766e_901e
Which one of the following genetic disorders correspond to the description 'metabolic disorder affecting branched-chain amino acids'.
A. Beta-Thalassemia Incorrect B. Duchenne muscular dystrophy Incorrect C. Galactosemia Incorrect D. Maple syrup urine disease Correct E. Philadelphia chromosome Incorrect MC784a_0145
Which one of the following genetic disorders correspond to the description 'also known as 47,XXX, is a genetic disorder that results in a female that has three X chromosomes'.
A. Beta-Thalassemia Incorrect B. Cystic fibrosis Incorrect C. Down syndrome Incorrect D. Galactosemia Incorrect E. Triple X syndrome Correct MC784a_10d0
Which one of the following genetic disorders correspond to the description 'also known as 47,XXX, is a genetic disorder that results in a female that has three X chromosomes'.
A. Achondroplasia Incorrect B. Beta-Thalassemia Incorrect C. Cystic fibrosis Incorrect D. Duchenne muscular dystrophy Incorrect E. Triple X syndrome Correct MC784a_60dd
Which one of the following genetic disorders correspond to the description 'also known as 47,XXX, is a genetic disorder that results in a female that has three X chromosomes'.
A. Cystic fibrosis Incorrect B. Klinefelter syndrome Incorrect C. Patau syndrome Incorrect D. Triple X syndrome Correct E. Turner syndrome Incorrect MC7a23_1da5
Which one of the following genetic disorders correspond to the description 'a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13'.
A. Achondroplasia Incorrect B. Down syndrome Incorrect C. Patau syndrome Correct D. Philadelphia chromosome Incorrect E. Turner syndrome Incorrect MC7a23_3685
Which one of the following genetic disorders correspond to the description 'a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13'.
A. Angelman syndrome Incorrect B. Beta-Thalassemia Incorrect C. Maple syrup urine disease Incorrect D. Patau syndrome Correct E. Tay-Sachs disease Incorrect MC7a23_c4bf
Which one of the following genetic disorders correspond to the description 'a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13'.
A. Angelman syndrome Incorrect B. Hemophilia Incorrect C. Patau syndrome Correct D. Tay-Sachs disease Incorrect E. Turner syndrome Incorrect MC7a23_d702
Which one of the following genetic disorders correspond to the description 'a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13'.
A. Angelman syndrome Incorrect B. Cri du chat syndrome Incorrect C. Cystic fibrosis Incorrect D. Patau syndrome Correct E. Turner syndrome Incorrect MC8048_6fa1
Which one of the following genetic disorders correspond to the description 'genetic disorder caused by the presence of all or part of a third copy of chromosome 21'.
A. Down syndrome Correct B. Philadelphia chromosome Incorrect C. Tay-Sachs disease Incorrect D. Triple X syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MC84a9_055c
Which one of the following genetic disorders correspond to the description 'genetic condition caused by a deletion of a group of genes located on chromosome number 11'.
A. Beta-Thalassemia Incorrect B. Cri du chat syndrome Incorrect C. Philadelphia chromosome Incorrect D. Sickle-cell anemia Incorrect E. WAGR syndrome Correct MC84a9_ef36
Which one of the following genetic disorders correspond to the description 'genetic condition caused by a deletion of a group of genes located on chromosome number 11'.
A. DiGeorge syndrome Incorrect B. Down syndrome Incorrect C. Fragile X syndrome Incorrect D. Hemophilia Incorrect E. WAGR syndrome Correct MC9acf_1ca6
Which one of the following genetic disorders correspond to the description 'multi-systemic genetic disorder that affects the connective tissue'.
A. Beta-Thalassemia Incorrect B. Fragile X syndrome Incorrect C. Hemophilia Incorrect D. Marfan syndrome Correct E. Philadelphia chromosome Incorrect MC9acf_4435
Which one of the following genetic disorders correspond to the description 'multi-systemic genetic disorder that affects the connective tissue'.
A. Beta-Thalassemia Incorrect B. Edwards syndrome Incorrect C. Maple syrup urine disease Incorrect D. Marfan syndrome Correct E. WAGR syndrome Incorrect MC9b35_dfb7
Which one of the following genetic disorders correspond to the description 'disorder that is due to a missing piece (deletion) of a specific part of chromosome 22'.
A. DiGeorge syndrome Correct B. Duchenne muscular dystrophy Incorrect C. Huntington's disease Incorrect D. Klinefelter syndrome Incorrect E. Patau syndrome Incorrect MC9b35_f9bf
Which one of the following genetic disorders correspond to the description 'disorder that is due to a missing piece (deletion) of a specific part of chromosome 22'.
A. Achondroplasia Incorrect B. Angelman syndrome Incorrect C. Cri du chat syndrome Incorrect D. DiGeorge syndrome Correct E. Galactosemia Incorrect MC9b8c_cef9
Which one of the following genetic disorders correspond to the description 'result of a random error that causes a male to be born with an extra X chromosome'.
A. Achondroplasia Incorrect B. DiGeorge syndrome Incorrect C. Huntington's disease Incorrect D. Klinefelter syndrome Correct E. Tay-Sachs disease Incorrect MCa1ff_4601
Which one of the following genetic disorders correspond to the description 'disorder that is due to a missing piece (deletion) of a specific part of chromosome 5'.
A. Cri du chat syndrome Correct B. DiGeorge syndrome Incorrect C. Philadelphia chromosome Incorrect D. Turner syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MCa9dd_3c70
Which one of the following genetic disorders correspond to the description 'caused by duplications of the UBE3A gene located on chromosome 15'.
A. Angelman syndrome Correct B. DiGeorge syndrome Incorrect C. Down syndrome Incorrect D. Tay-Sachs disease Incorrect E. Turner syndrome Incorrect MCa9dd_a935
Which one of the following genetic disorders correspond to the description 'caused by duplications of the UBE3A gene located on chromosome 15'.
A. Angelman syndrome Correct B. Cri du chat syndrome Incorrect C. Edwards syndrome Incorrect D. Sickle-cell anemia Incorrect E. Wolf-Hirschhorn syndrome Incorrect MCbe00_f58d
Which one of the following genetic disorders correspond to the description 'chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 18th chromosome'.
A. Beta-Thalassemia Incorrect B. Edwards syndrome Correct C. Marfan syndrome Incorrect D. Phenylketonuria Incorrect E. Triple X syndrome Incorrect MCc05d_b801
Which one of the following genetic disorders correspond to the description 'genetic condition caused by a deletion of a group of genes located on chromosome number 4'.
A. Angelman syndrome Incorrect B. DiGeorge syndrome Incorrect C. Galactosemia Incorrect D. Phenylketonuria Incorrect E. Wolf-Hirschhorn syndrome Correct MCc05d_d6f5
Which one of the following genetic disorders correspond to the description 'genetic condition caused by a deletion of a group of genes located on chromosome number 4'.
A. Angelman syndrome Incorrect B. Fragile X syndrome Incorrect C. Maple syrup urine disease Incorrect D. Turner syndrome Incorrect E. Wolf-Hirschhorn syndrome Correct MCc4f4_3e5a
Which one of the following genetic disorders correspond to the description 'disorder that is due to a missing piece (deletion) of a specific part of chromosome 4'.
A. Achondroplasia Incorrect B. Down syndrome Incorrect C. Hemophilia Incorrect D. Sickle-cell anemia Incorrect E. Wolf-Hirschhorn syndrome Correct MCc4f4_4bad
Which one of the following genetic disorders correspond to the description 'disorder that is due to a missing piece (deletion) of a specific part of chromosome 4'.
A. Angelman syndrome Incorrect B. Cri du chat syndrome Incorrect C. Patau syndrome Incorrect D. Prader-Willi syndrome Incorrect E. Wolf-Hirschhorn syndrome Correct MCcc2b_048a
Which one of the following genetic disorders correspond to the description 'chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 21st chromosome'.
A. Beta-Thalassemia Incorrect B. Down syndrome Correct C. Huntington's disease Incorrect D. Sickle-cell anemia Incorrect E. Turner syndrome Incorrect MCcc2b_33dd
Which one of the following genetic disorders correspond to the description 'chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 21st chromosome'.
A. Down syndrome Correct B. Klinefelter syndrome Incorrect C. Patau syndrome Incorrect D. Philadelphia chromosome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MCcc2b_ddbb
Which one of the following genetic disorders correspond to the description 'chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 21st chromosome'.
A. Achondroplasia Incorrect B. Down syndrome Correct C. Hemophilia Incorrect D. Klinefelter syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MCcc2b_f454
Which one of the following genetic disorders correspond to the description 'chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 21st chromosome'.
A. Beta-Thalassemia Incorrect B. Down syndrome Correct C. Klinefelter syndrome Incorrect D. Marfan syndrome Incorrect E. Triple X syndrome Incorrect MCcd05_714b
Which one of the following genetic disorders correspond to the description 'a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 18'.
A. Duchenne muscular dystrophy Incorrect B. Edwards syndrome Correct C. Fragile X syndrome Incorrect D. Sickle-cell anemia Incorrect E. Turner syndrome Incorrect MCcd05_e738
Which one of the following genetic disorders correspond to the description 'a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 18'.
A. Beta-Thalassemia Incorrect B. Edwards syndrome Correct C. Patau syndrome Incorrect D. Sickle-cell anemia Incorrect E. Triple X syndrome Incorrect MCd837_c8df
Which one of the following genetic disorders correspond to the description 'cancerous chromosomal abnormality that is manifested as a shortened version of human chromosome 22'.
A. Huntington's disease Incorrect B. Philadelphia chromosome Correct C. Prader-Willi syndrome Incorrect D. Sickle-cell anemia Incorrect E. Triple X syndrome Incorrect MCd8d7_4b57
Which one of the following genetic disorders correspond to the description 'disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15'.
A. Achondroplasia Incorrect B. Angelman syndrome Correct C. Beta-Thalassemia Incorrect D. Duchenne muscular dystrophy Incorrect E. Tay-Sachs disease Incorrect MCd8d7_67b7
Which one of the following genetic disorders correspond to the description 'disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15'.
A. Achondroplasia Incorrect B. Angelman syndrome Correct C. Cri du chat syndrome Incorrect D. Duchenne muscular dystrophy Incorrect E. Klinefelter syndrome Incorrect MCde15_2077
Which one of the following genetic disorders correspond to the description 'people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase'.
A. Cri du chat syndrome Incorrect B. Galactosemia Incorrect C. Sickle-cell anemia Incorrect D. Tay-Sachs disease Correct E. WAGR syndrome Incorrect MCde15_66aa
Which one of the following genetic disorders correspond to the description 'people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase'.
A. Beta-Thalassemia Incorrect B. Down syndrome Incorrect C. Hemophilia Incorrect D. Tay-Sachs disease Correct E. Wolf-Hirschhorn syndrome Incorrect MCdfb6_03f9
Which one of the following genetic disorders correspond to the description 'affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells'.
A. Edwards syndrome Incorrect B. Fragile X syndrome Incorrect C. Patau syndrome Incorrect D. Prader-Willi syndrome Incorrect E. Sickle-cell anemia Correct MCdfb6_e738
Which one of the following genetic disorders correspond to the description 'affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells'.
A. Beta-Thalassemia Incorrect B. Edwards syndrome Incorrect C. Patau syndrome Incorrect D. Sickle-cell anemia Correct E. Triple X syndrome Incorrect MCe347_001d
Which one of the following genetic disorders correspond to the description 'result of a random error that causes a person to be born with an extra chromosome 13'.
A. Beta-Thalassemia Incorrect B. Cri du chat syndrome Incorrect C. Huntington's disease Incorrect D. Patau syndrome Correct E. Philadelphia chromosome Incorrect MCe347_22fa
Which one of the following genetic disorders correspond to the description 'result of a random error that causes a person to be born with an extra chromosome 13'.
A. Beta-Thalassemia Incorrect B. Duchenne muscular dystrophy Incorrect C. Patau syndrome Correct D. WAGR syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MCe6ec_5e3c
Which one of the following genetic disorders correspond to the description 'an inherited bleeding disorder in which the blood does NOT clot properly'.
A. Beta-Thalassemia Incorrect B. Cystic fibrosis Incorrect C. Down syndrome Incorrect D. Hemophilia Correct E. Philadelphia chromosome Incorrect MCe6ec_e32d
Which one of the following genetic disorders correspond to the description 'an inherited bleeding disorder in which the blood does NOT clot properly'.
A. Cystic fibrosis Incorrect B. Duchenne muscular dystrophy Incorrect C. Hemophilia Correct D. Tay-Sachs disease Incorrect E. WAGR syndrome Incorrect MCe930_0acd
Which one of the following genetic disorders correspond to the description 'a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21'.
A. Down syndrome Correct B. Huntington's disease Incorrect C. Klinefelter syndrome Incorrect D. Marfan syndrome Incorrect E. Tay-Sachs disease Incorrect MCe930_48dc
Which one of the following genetic disorders correspond to the description 'a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21'.
A. Down syndrome Correct B. Hemophilia Incorrect C. Huntington's disease Incorrect D. Philadelphia chromosome Incorrect E. Prader-Willi syndrome Incorrect MCe930_b2e1
Which one of the following genetic disorders correspond to the description 'a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21'.
A. Angelman syndrome Incorrect B. DiGeorge syndrome Incorrect C. Down syndrome Correct D. Marfan syndrome Incorrect E. Sickle-cell anemia Incorrect MCf390_9144
Which one of the following genetic disorders correspond to the description 'disorder that affects the muscles, leading to muscle wasting that gets worse over time'.
A. Angelman syndrome Incorrect B. Cri du chat syndrome Incorrect C. Duchenne muscular dystrophy Correct D. Hemophilia Incorrect E. Sickle-cell anemia Incorrect MCf824_0773
Which one of the following genetic disorders correspond to the description 'a genetic disorder caused by a loss of function of specific genes on chromosome 15'.
A. Galactosemia Incorrect B. Huntington's disease Incorrect C. Marfan syndrome Incorrect D. Prader-Willi syndrome Correct E. WAGR syndrome Incorrect MCf824_68d5
Which one of the following genetic disorders correspond to the description 'a genetic disorder caused by a loss of function of specific genes on chromosome 15'.
A. Cystic fibrosis Incorrect B. Galactosemia Incorrect C. Marfan syndrome Incorrect D. Philadelphia chromosome Incorrect E. Prader-Willi syndrome Correct MCf824_9fc0
Which one of the following genetic disorders correspond to the description 'a genetic disorder caused by a loss of function of specific genes on chromosome 15'.
A. Beta-Thalassemia Incorrect B. Duchenne muscular dystrophy Incorrect C. Klinefelter syndrome Incorrect D. Prader-Willi syndrome Correct E. WAGR syndrome Incorrect MCfa9e_3a42
Which one of the following genetic disorders correspond to the description 'usually include a high-pitched cat-like cry, mental disability, delayed development, distinctive facial features, widely-spaced eyes'.
A. Achondroplasia Incorrect B. Cri du chat syndrome Correct C. Cystic fibrosis Incorrect D. Prader-Willi syndrome Incorrect E. Sickle-cell anemia Incorrect MCfa9e_8c03
Which one of the following genetic disorders correspond to the description 'usually include a high-pitched cat-like cry, mental disability, delayed development, distinctive facial features, widely-spaced eyes'.
A. Cri du chat syndrome Correct B. DiGeorge syndrome Incorrect C. Fragile X syndrome Incorrect D. Prader-Willi syndrome Incorrect E. Tay-Sachs disease Incorrect MCfaab_81d1
Which one of the following genetic disorders correspond to the description 'a genetic condition in females which there are three copies of the X chromosome'.
A. Duchenne muscular dystrophy Incorrect B. Huntington's disease Incorrect C. Patau syndrome Incorrect D. Triple X syndrome Correct E. Wolf-Hirschhorn syndrome Incorrect MCfaab_907a
Which one of the following genetic disorders correspond to the description 'a genetic condition in females which there are three copies of the X chromosome'.
A. Achondroplasia Incorrect B. Cystic fibrosis Incorrect C. Philadelphia chromosome Incorrect D. Prader-Willi syndrome Incorrect E. Triple X syndrome Correct MCff1a_750c
Which one of the following genetic disorders correspond to the description 'also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome'.
A. Galactosemia Incorrect B. Klinefelter syndrome Correct C. Sickle-cell anemia Incorrect D. WAGR syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MCff1a_7994
Which one of the following genetic disorders correspond to the description 'also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome'.
A. Beta-Thalassemia Incorrect B. Klinefelter syndrome Correct C. Prader-Willi syndrome Incorrect D. Turner syndrome Incorrect E. WAGR syndrome Incorrect MCff1a_efd7
Which one of the following genetic disorders correspond to the description 'also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome'.
A. Klinefelter syndrome Correct B. Maple syrup urine disease Incorrect C. Sickle-cell anemia Incorrect D. Tay-Sachs disease Incorrect E. Triple X syndrome Incorrect MCff26_435e
Which one of the following genetic disorders correspond to the description 'genetic metabolic disorder that increases the body's levels of phenylalanine'.
A. Fragile X syndrome Incorrect B. Huntington's disease Incorrect C. Phenylketonuria Correct D. Triple X syndrome Incorrect E. Wolf-Hirschhorn syndrome Incorrect MCff26_4fac
Which one of the following genetic disorders correspond to the description 'genetic metabolic disorder that increases the body's levels of phenylalanine'.
A. Edwards syndrome Incorrect B. Fragile X syndrome Incorrect C. Huntington's disease Incorrect D. Klinefelter syndrome Incorrect E. Phenylketonuria Correct