8894_6964
Which one of the following genetic disorders correspond to the description 'genetic metabolic disorder that increases the body's levels of phenylalanine'.
Cystic fibrosis Incorrect Galactosemia Incorrect Patau syndrome Incorrect Phenylketonuria Correct MCb129_1cc0
Which one of the following genetic disorders correspond to the description 'an inherited bleeding disorder in which the blood does NOT clot properly'.
Cri du chat syndrome Incorrect Hemophilia Correct Huntington's disease Incorrect Sickle-cell anemia Incorrect MC0ce9_b6f8
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'.
Down syndrome Correct Galactosemia Incorrect Philadelphia chromosome Incorrect Turner syndrome Incorrect MC153a_7b11
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'.
Achondroplasia Incorrect Down syndrome Incorrect Galactosemia Incorrect Triple X syndrome Correct MCaff5_5cfb
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'.
Achondroplasia Incorrect Hemophilia Incorrect Marfan syndrome Correct Sickle-cell anemia Incorrect MCe6d9_6ad7
Which one of the following genetic disorders correspond to the description 'reduced hemoglobin proteins that result in variable outcomes including severe anemia'.
Beta-Thalassemia Correct Maple syrup urine disease Incorrect Sickle-cell anemia Incorrect Tay-Sachs disease Incorrect MCcc52_f19a
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'.
Down syndrome Incorrect Hemophilia Incorrect Klinefelter syndrome Correct WAGR syndrome Incorrect MC153a_a68f
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'.
Cri du chat syndrome Incorrect Huntington's disease Incorrect Philadelphia chromosome Incorrect Triple X syndrome Correct MC20b6_97e6
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'.
Achondroplasia Incorrect Cri du chat syndrome Correct Fragile X syndrome Incorrect Sickle-cell anemia Incorrect MC898c_cdc2
Which one of the following genetic disorders correspond to the description 'autosomal recessive genetic disorder affecting most critically the lungs'.
Cystic fibrosis Correct Huntington's disease Incorrect Marfan syndrome Incorrect WAGR syndrome Incorrect MCc735_8af3
Which one of the following genetic disorders correspond to the description 'gets its name from the distinctive sweet odor of affected infants' urine'.
Angelman syndrome Incorrect Beta-Thalassemia Incorrect Fragile X syndrome Incorrect Maple syrup urine disease Correct MC16de_6b96
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'.
Beta-Thalassemia Incorrect Down syndrome Incorrect Sickle-cell anemia Correct WAGR syndrome Incorrect MCfcfd_2ea2
Which one of the following genetic disorders correspond to the description 'caused by duplications of the UBE3A gene located on chromosome 15'.
Angelman syndrome Correct Huntington's disease Incorrect Prader-Willi syndrome Incorrect Tay-Sachs disease Incorrect MCfcfd_6bcc
Which one of the following genetic disorders correspond to the description 'caused by duplications of the UBE3A gene located on chromosome 15'.
Angelman syndrome Correct Cystic fibrosis Incorrect DiGeorge syndrome Incorrect Fragile X syndrome Incorrect MC20b6_861e
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'.
Cri du chat syndrome Correct DiGeorge syndrome Incorrect Duchenne muscular dystrophy Incorrect Fragile X syndrome Incorrect MC20b6_8200
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'.
Cri du chat syndrome Correct Hemophilia Incorrect Marfan syndrome Incorrect Prader-Willi syndrome Incorrect MC20b6_8fc0
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'.
Cri du chat syndrome Correct Edwards syndrome Incorrect Patau syndrome Incorrect Prader-Willi syndrome Incorrect MCe6d9_583d
Which one of the following genetic disorders correspond to the description 'reduced hemoglobin proteins that result in variable outcomes including severe anemia'.
Beta-Thalassemia Correct Cystic fibrosis Incorrect Klinefelter syndrome Incorrect Philadelphia chromosome Incorrect MC864c_0134
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'.
Cri du chat syndrome Incorrect Phenylketonuria Correct Philadelphia chromosome Incorrect Tay-Sachs disease Incorrect MCb880_0374
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 5 is missing'.
Cri du chat syndrome Correct Cystic fibrosis Incorrect Down syndrome Incorrect WAGR syndrome Incorrect MCf23c_6b1a
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'.
Cri du chat syndrome Incorrect Hemophilia Incorrect Huntington's disease Incorrect Prader-Willi syndrome Correct MC2189_85b7
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 15'.
Achondroplasia Incorrect Angelman syndrome Incorrect Klinefelter syndrome Incorrect Prader-Willi syndrome Correct MC12c1_0bc3
Which one of the following genetic disorders correspond to the description 'metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly'.
DiGeorge syndrome Incorrect Galactosemia Correct Klinefelter syndrome Incorrect Turner syndrome Incorrect MC0bc2_b6f7
Which one of the following genetic disorders correspond to the description 'also known as monosomy X, includes a number of typical physical features observed such as webbed neck'.
DiGeorge syndrome Incorrect Maple syrup urine disease Incorrect Philadelphia chromosome Incorrect Turner syndrome Correct MC898c_c18d
Which one of the following genetic disorders correspond to the description 'autosomal recessive genetic disorder affecting most critically the lungs'.
Cystic fibrosis Correct Phenylketonuria Incorrect Triple X syndrome Incorrect WAGR syndrome Incorrect MC90c4_a017
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 18'.
DiGeorge syndrome Incorrect Edwards syndrome Correct Hemophilia Incorrect Wolf-Hirschhorn syndrome Incorrect MCfcfd_3017
Which one of the following genetic disorders correspond to the description 'caused by duplications of the UBE3A gene located on chromosome 15'.
Angelman syndrome Correct Klinefelter syndrome Incorrect Triple X syndrome Incorrect Wolf-Hirschhorn syndrome Incorrect MC182d_62c7
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'.
Beta-Thalassemia Incorrect Cri du chat syndrome Correct Philadelphia chromosome Incorrect Wolf-Hirschhorn syndrome Incorrect MCe6a1_c6d6
Which one of the following genetic disorders correspond to the description 'inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine'.
Angelman syndrome Incorrect Beta-Thalassemia Incorrect Down syndrome Incorrect Phenylketonuria Correct MC2189_56c0
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 15'.
Achondroplasia Incorrect Prader-Willi syndrome Correct Sickle-cell anemia Incorrect Tay-Sachs disease Incorrect MCb4f1_67af
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'.
Beta-Thalassemia Incorrect Down syndrome Correct Fragile X syndrome Incorrect Marfan syndrome Incorrect MC5924_d292
Which one of the following genetic disorders correspond to the description 'multi-systemic genetic disorder that affects the connective tissue'.
Cystic fibrosis Incorrect Galactosemia Incorrect Klinefelter syndrome Incorrect Marfan syndrome Correct MC5c24_50ec
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'.
Cystic fibrosis Correct Galactosemia Incorrect Maple syrup urine disease Incorrect Patau syndrome Incorrect MC0bc2_fa9f
Which one of the following genetic disorders correspond to the description 'also known as monosomy X, includes a number of typical physical features observed such as webbed neck'.
Angelman syndrome Incorrect Fragile X syndrome Incorrect Sickle-cell anemia Incorrect Turner syndrome Correct MC3c6e_151c
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 11 is missing'.
Maple syrup urine disease Incorrect Tay-Sachs disease Incorrect WAGR syndrome Correct Wolf-Hirschhorn syndrome Incorrect MC2189_68a3
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 15'.
Galactosemia Incorrect Huntington's disease Incorrect Marfan syndrome Incorrect Prader-Willi syndrome Correct MC9f25_f5f6
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'.
Down syndrome Incorrect Duchenne muscular dystrophy Correct Triple X syndrome Incorrect Turner syndrome Incorrect MC539c_1616
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'.
Achondroplasia Incorrect DiGeorge syndrome Correct Maple syrup urine disease Incorrect WAGR syndrome Incorrect MC1be3_7738
Which one of the following genetic disorders correspond to the description 'disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain'.
Edwards syndrome Incorrect Fragile X syndrome Incorrect Huntington's disease Correct Prader-Willi syndrome Incorrect MC9f25_303f
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'.
Cri du chat syndrome Incorrect Cystic fibrosis Incorrect Duchenne muscular dystrophy Correct Hemophilia Incorrect MC153a_ec2c
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'.
Fragile X syndrome Incorrect Maple syrup urine disease Incorrect Triple X syndrome Correct Wolf-Hirschhorn syndrome Incorrect MC0bc2_09f7
Which one of the following genetic disorders correspond to the description 'also known as monosomy X, includes a number of typical physical features observed such as webbed neck'.
Down syndrome Incorrect Edwards syndrome Incorrect Patau syndrome Incorrect Turner syndrome Correct MC539c_fe8d
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'.
Cri du chat syndrome Incorrect DiGeorge syndrome Correct Marfan syndrome Incorrect Wolf-Hirschhorn syndrome Incorrect MC27e2_8115
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'.
Edwards syndrome Incorrect Patau syndrome Correct Phenylketonuria Incorrect Wolf-Hirschhorn syndrome Incorrect MCaff5_ddad
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'.
Huntington's disease Incorrect Marfan syndrome Correct Patau syndrome Incorrect Turner syndrome Incorrect MCc323_93e6
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'.
Cri du chat syndrome Incorrect Down syndrome Correct Turner syndrome Incorrect Wolf-Hirschhorn syndrome Incorrect MC2189_cabb
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 15'.
Achondroplasia Incorrect Cri du chat syndrome Incorrect Prader-Willi syndrome Correct Sickle-cell anemia Incorrect MC1be3_a421
Which one of the following genetic disorders correspond to the description 'disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain'.
Cri du chat syndrome Incorrect Duchenne muscular dystrophy Incorrect Edwards syndrome Incorrect Huntington's disease Correct MCd135_935b
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'.
Beta-Thalassemia Incorrect DiGeorge syndrome Incorrect Klinefelter syndrome Incorrect Wolf-Hirschhorn syndrome Correct MCf23c_c878
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'.
DiGeorge syndrome Incorrect Edwards syndrome Incorrect Galactosemia Incorrect Prader-Willi syndrome Correct MCb129_f861
Which one of the following genetic disorders correspond to the description 'an inherited bleeding disorder in which the blood does NOT clot properly'.
Edwards syndrome Incorrect Fragile X syndrome Incorrect Galactosemia Incorrect Hemophilia Correct MC3c6e_e7be
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 11 is missing'.
Duchenne muscular dystrophy Incorrect Maple syrup urine disease Incorrect Turner syndrome Incorrect WAGR syndrome Correct MCaff5_bfbc
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'.
Duchenne muscular dystrophy Incorrect Marfan syndrome Correct Patau syndrome Incorrect Philadelphia chromosome Incorrect MCa584_4538
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'.
Galactosemia Incorrect Hemophilia Incorrect Triple X syndrome Incorrect WAGR syndrome Correct MC90c4_0ad7
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 18'.
Angelman syndrome Incorrect Down syndrome Incorrect Edwards syndrome Correct Sickle-cell anemia Incorrect MCba7c_56b2
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'.
Beta-Thalassemia Incorrect Klinefelter syndrome Incorrect Sickle-cell anemia Incorrect Turner syndrome Correct MCd5e8_5cb1
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'.
Duchenne muscular dystrophy Incorrect Fragile X syndrome Incorrect Patau syndrome Incorrect Triple X syndrome Correct MCd135_fd7f
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'.
Duchenne muscular dystrophy Incorrect Sickle-cell anemia Incorrect Tay-Sachs disease Incorrect Wolf-Hirschhorn syndrome Correct MC153a_5ce1
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'.
Down syndrome Incorrect Galactosemia Incorrect Marfan syndrome Incorrect Triple X syndrome Correct MC0bc2_3d44
Which one of the following genetic disorders correspond to the description 'also known as monosomy X, includes a number of typical physical features observed such as webbed neck'.
Edwards syndrome Incorrect Philadelphia chromosome Incorrect Triple X syndrome Incorrect Turner syndrome Correct MC7f7a_f1ca
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'.
Cri du chat syndrome Incorrect Edwards syndrome Correct Galactosemia Incorrect Klinefelter syndrome Incorrect MC898c_4add
Which one of the following genetic disorders correspond to the description 'autosomal recessive genetic disorder affecting most critically the lungs'.
Cystic fibrosis Correct Edwards syndrome Incorrect Maple syrup urine disease Incorrect Turner syndrome Incorrect MCf23c_8041
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'.
Cri du chat syndrome Incorrect Hemophilia Incorrect Prader-Willi syndrome Correct WAGR syndrome Incorrect MC28dc_6f54
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'.
Edwards syndrome Correct Patau syndrome Incorrect Philadelphia chromosome Incorrect WAGR syndrome Incorrect MC0ce9_86b6
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'.
Down syndrome Correct Phenylketonuria Incorrect Prader-Willi syndrome Incorrect WAGR syndrome Incorrect MCc323_2902
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'.
Down syndrome Correct Hemophilia Incorrect Klinefelter syndrome Incorrect Phenylketonuria Incorrect MCd5e8_37ed
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'.
Fragile X syndrome Incorrect Maple syrup urine disease Incorrect Triple X syndrome Correct WAGR syndrome Incorrect MCeda9_391f
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'.
Angelman syndrome Incorrect Fragile X syndrome Incorrect Huntington's disease Incorrect Tay-Sachs disease Correct MCf23c_af92
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'.
Duchenne muscular dystrophy Incorrect Edwards syndrome Incorrect Prader-Willi syndrome Correct Tay-Sachs disease Incorrect MCc323_2914
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'.
Beta-Thalassemia Incorrect DiGeorge syndrome Incorrect Down syndrome Correct Prader-Willi syndrome Incorrect MCeda9_db94
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'.
Hemophilia Incorrect Klinefelter syndrome Incorrect Tay-Sachs disease Correct WAGR syndrome Incorrect MCa584_ce30
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'.
Klinefelter syndrome Incorrect Patau syndrome Incorrect Triple X syndrome Incorrect WAGR syndrome Correct MCe6a1_6d6f
Which one of the following genetic disorders correspond to the description 'inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine'.
Down syndrome Incorrect Duchenne muscular dystrophy Incorrect Fragile X syndrome Incorrect Phenylketonuria Correct MCaff5_abef
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'.
Beta-Thalassemia Incorrect Marfan syndrome Correct Prader-Willi syndrome Incorrect WAGR syndrome Incorrect MCe6d9_da08
Which one of the following genetic disorders correspond to the description 'reduced hemoglobin proteins that result in variable outcomes including severe anemia'.
Beta-Thalassemia Correct Fragile X syndrome Incorrect Hemophilia Incorrect Marfan syndrome Incorrect MCf23c_0af5
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'.
Duchenne muscular dystrophy Incorrect Fragile X syndrome Incorrect Philadelphia chromosome Incorrect Prader-Willi syndrome Correct MCba7c_2cef
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'.
Angelman syndrome Incorrect Hemophilia Incorrect Prader-Willi syndrome Incorrect Turner syndrome Correct MC35e7_0c0d
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'.
Cri du chat syndrome Incorrect Down syndrome Incorrect Klinefelter syndrome Correct Tay-Sachs disease Incorrect MCb129_aff1
Which one of the following genetic disorders correspond to the description 'an inherited bleeding disorder in which the blood does NOT clot properly'.
Fragile X syndrome Incorrect Hemophilia Correct Philadelphia chromosome Incorrect Prader-Willi syndrome Incorrect MCa584_e91c
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'.
Cystic fibrosis Incorrect Maple syrup urine disease Incorrect WAGR syndrome Correct Wolf-Hirschhorn syndrome Incorrect MCb4f1_2b55
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'.
Down syndrome Correct Galactosemia Incorrect Klinefelter syndrome Incorrect Triple X syndrome Incorrect MC153a_f144
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'.
Cri du chat syndrome Incorrect Marfan syndrome Incorrect Triple X syndrome Correct WAGR syndrome Incorrect MC20b6_8993
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'.
Angelman syndrome Incorrect Cri du chat syndrome Correct Fragile X syndrome Incorrect Marfan syndrome Incorrect MC182d_172e
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'.
Cri du chat syndrome Correct Fragile X syndrome Incorrect Patau syndrome Incorrect Triple X syndrome Incorrect MC5924_8ca1
Which one of the following genetic disorders correspond to the description 'multi-systemic genetic disorder that affects the connective tissue'.
Achondroplasia Incorrect DiGeorge syndrome Incorrect Marfan syndrome Correct WAGR syndrome Incorrect MC153a_15ce
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'.
Fragile X syndrome Incorrect Maple syrup urine disease Incorrect Patau syndrome Incorrect Triple X syndrome Correct MC9f25_5c32
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'.
Angelman syndrome Incorrect Duchenne muscular dystrophy Correct Sickle-cell anemia Incorrect Triple X syndrome Incorrect MC90c4_698b
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 18'.
DiGeorge syndrome Incorrect Edwards syndrome Correct Galactosemia Incorrect Philadelphia chromosome Incorrect MC3ad4_e5d9
Which one of the following genetic disorders correspond to the description 'a genetic condition involving changes in part of the X chromosome'.
Down syndrome Incorrect Fragile X syndrome Correct Marfan syndrome Incorrect Sickle-cell anemia Incorrect MC864c_a820
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'.
Beta-Thalassemia Incorrect Down syndrome Incorrect Phenylketonuria Correct WAGR syndrome Incorrect MC7f7a_5b19
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'.
Achondroplasia Incorrect Edwards syndrome Correct Huntington's disease Incorrect Sickle-cell anemia Incorrect MC28dc_259d
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'.
Edwards syndrome Correct Prader-Willi syndrome Incorrect Triple X syndrome Incorrect Wolf-Hirschhorn syndrome Incorrect MC5c24_d9a6
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'.
Cri du chat syndrome Incorrect Cystic fibrosis Correct Patau syndrome Incorrect Phenylketonuria Incorrect MC27e2_625a
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'.
Down syndrome Incorrect Hemophilia Incorrect Patau syndrome Correct Sickle-cell anemia Incorrect MCe716_095f
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'.
Edwards syndrome Correct Sickle-cell anemia Incorrect Turner syndrome Incorrect Wolf-Hirschhorn syndrome Incorrect MCb129_0a8c
Which one of the following genetic disorders correspond to the description 'an inherited bleeding disorder in which the blood does NOT clot properly'.
Cri du chat syndrome Incorrect Hemophilia Correct Sickle-cell anemia Incorrect Tay-Sachs disease Incorrect MC5c24_b40f
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'.
Beta-Thalassemia Incorrect Cystic fibrosis Correct Triple X syndrome Incorrect Turner syndrome Incorrect MC539c_c330
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'.
Achondroplasia Incorrect Cystic fibrosis Incorrect DiGeorge syndrome Correct Triple X syndrome Incorrect MCfdc3_a12a
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'.
Angelman syndrome Correct DiGeorge syndrome Incorrect Philadelphia chromosome Incorrect Turner syndrome Incorrect MC9ffa_cbb1
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'.
Achondroplasia Incorrect Klinefelter syndrome Incorrect Marfan syndrome Incorrect Patau syndrome Correct MC898c_d009
Which one of the following genetic disorders correspond to the description 'autosomal recessive genetic disorder affecting most critically the lungs'.
Achondroplasia Incorrect Cystic fibrosis Correct Marfan syndrome Incorrect Patau syndrome Incorrect MC1be3_270b
Which one of the following genetic disorders correspond to the description 'disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain'.
Achondroplasia Incorrect Fragile X syndrome Incorrect Huntington's disease Correct Marfan syndrome Incorrect MC217f_0e72
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 22 is missing'.
DiGeorge syndrome Correct Galactosemia Incorrect Maple syrup urine disease Incorrect Wolf-Hirschhorn syndrome Incorrect MC217f_3655
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 22 is missing'.
Angelman syndrome Incorrect DiGeorge syndrome Correct Klinefelter syndrome Incorrect Sickle-cell anemia Incorrect MCd5e8_4aca
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'.
Angelman syndrome Incorrect DiGeorge syndrome Incorrect Hemophilia Incorrect Triple X syndrome Correct MC2596_3112
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'.
Achondroplasia Correct Cystic fibrosis Incorrect Edwards syndrome Incorrect Fragile X syndrome Incorrect MC44bb_f671
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'.
Duchenne muscular dystrophy Incorrect Edwards syndrome Incorrect Hemophilia Incorrect Tay-Sachs disease Correct MCf23c_4598
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'.
Cystic fibrosis Incorrect Klinefelter syndrome Incorrect Prader-Willi syndrome Correct WAGR syndrome Incorrect MCd135_9e65
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'.
Down syndrome Incorrect Tay-Sachs disease Incorrect Turner syndrome Incorrect Wolf-Hirschhorn syndrome Correct MC0ce9_e264
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'.
Angelman syndrome Incorrect Down syndrome Correct Klinefelter syndrome Incorrect Maple syrup urine disease Incorrect MC90c4_f4d4
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 18'.
DiGeorge syndrome Incorrect Edwards syndrome Correct Philadelphia chromosome Incorrect Triple X syndrome Incorrect MCba7c_4b46
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'.
Duchenne muscular dystrophy Incorrect Sickle-cell anemia Incorrect Triple X syndrome Incorrect Turner syndrome Correct MC27e2_f1b3
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'.
Edwards syndrome Incorrect Patau syndrome Correct Philadelphia chromosome Incorrect Prader-Willi syndrome Incorrect MCe716_68f4
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'.
Edwards syndrome Correct Hemophilia Incorrect Huntington's disease Incorrect Maple syrup urine disease Incorrect MCc735_4d61
Which one of the following genetic disorders correspond to the description 'gets its name from the distinctive sweet odor of affected infants' urine'.
Beta-Thalassemia Incorrect Cri du chat syndrome Incorrect Klinefelter syndrome Incorrect Maple syrup urine disease Correct MC5924_4c9a
Which one of the following genetic disorders correspond to the description 'multi-systemic genetic disorder that affects the connective tissue'.
Achondroplasia Incorrect Down syndrome Incorrect Duchenne muscular dystrophy Incorrect Marfan syndrome Correct MCb4f1_5c1b
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'.
Achondroplasia Incorrect DiGeorge syndrome Incorrect Down syndrome Correct Triple X syndrome Incorrect MC864c_b0b6
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'.
DiGeorge syndrome Incorrect Phenylketonuria Correct Prader-Willi syndrome Incorrect Sickle-cell anemia Incorrect MCaff5_7cda
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'.
Hemophilia Incorrect Marfan syndrome Correct Philadelphia chromosome Incorrect Sickle-cell anemia Incorrect MCada0_b4e7
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 13th chromosome'.
Angelman syndrome Incorrect Galactosemia Incorrect Patau syndrome Correct Sickle-cell anemia Incorrect MCd5e8_bc5f
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'.
Cystic fibrosis Incorrect Philadelphia chromosome Incorrect Tay-Sachs disease Incorrect Triple X syndrome Correct MC8894_5278
Which one of the following genetic disorders correspond to the description 'genetic metabolic disorder that increases the body's levels of phenylalanine'.
Huntington's disease Incorrect Marfan syndrome Incorrect Phenylketonuria Correct Tay-Sachs disease Incorrect MCfcfd_a679
Which one of the following genetic disorders correspond to the description 'caused by duplications of the UBE3A gene located on chromosome 15'.
Angelman syndrome Correct Klinefelter syndrome Incorrect Prader-Willi syndrome Incorrect Turner syndrome Incorrect MCd135_3b32
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'.
Cystic fibrosis Incorrect Klinefelter syndrome Incorrect Philadelphia chromosome Incorrect Wolf-Hirschhorn syndrome Correct MC864c_4956
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'.
Klinefelter syndrome Incorrect Marfan syndrome Incorrect Phenylketonuria Correct Prader-Willi syndrome Incorrect MC7f7a_f048
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'.
Beta-Thalassemia Incorrect Edwards syndrome Correct Patau syndrome Incorrect Triple X syndrome Incorrect MCfa21_ad10
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'.
Prader-Willi syndrome Incorrect Tay-Sachs disease Incorrect WAGR syndrome Correct Wolf-Hirschhorn syndrome Incorrect MC5924_6559
Which one of the following genetic disorders correspond to the description 'multi-systemic genetic disorder that affects the connective tissue'.
Duchenne muscular dystrophy Incorrect Marfan syndrome Correct Philadelphia chromosome Incorrect Prader-Willi syndrome Incorrect MC45bd_1000
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'.
Edwards syndrome Incorrect Philadelphia chromosome Incorrect Sickle-cell anemia Incorrect Wolf-Hirschhorn syndrome Correct MCb303_a54c
Which one of the following genetic disorders correspond to the description 'metabolic disorder affecting branched-chain amino acids'.
Angelman syndrome Incorrect Beta-Thalassemia Incorrect Maple syrup urine disease Correct Turner syndrome Incorrect MC217f_d231
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 22 is missing'.
DiGeorge syndrome Correct Fragile X syndrome Incorrect Galactosemia Incorrect Turner syndrome Incorrect MC182d_42af
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'.
Cri du chat syndrome Correct Galactosemia Incorrect Hemophilia Incorrect Turner syndrome Incorrect MC16de_0efb
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'.
Angelman syndrome Incorrect Fragile X syndrome Incorrect Sickle-cell anemia Correct Wolf-Hirschhorn syndrome Incorrect MC9f25_33b6
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'.
Angelman syndrome Incorrect Down syndrome Incorrect Duchenne muscular dystrophy Correct Galactosemia Incorrect MCaff5_3511
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'.
Cystic fibrosis Incorrect Marfan syndrome Correct Prader-Willi syndrome Incorrect Triple X syndrome Incorrect MC28dc_a795
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'.
Achondroplasia Incorrect Angelman syndrome Incorrect Edwards syndrome Correct Patau syndrome Incorrect MCb4f1_1031
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'.
Down syndrome Correct Maple syrup urine disease Incorrect Marfan syndrome Incorrect WAGR syndrome Incorrect MCe6d9_7c63
Which one of the following genetic disorders correspond to the description 'reduced hemoglobin proteins that result in variable outcomes including severe anemia'.
Beta-Thalassemia Correct Hemophilia Incorrect Phenylketonuria Incorrect Triple X syndrome Incorrect MCfcfd_a9a2
Which one of the following genetic disorders correspond to the description 'caused by duplications of the UBE3A gene located on chromosome 15'.
Angelman syndrome Correct Cri du chat syndrome Incorrect Klinefelter syndrome Incorrect Maple syrup urine disease Incorrect MCada0_eab5
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 13th chromosome'.
Edwards syndrome Incorrect Klinefelter syndrome Incorrect Patau syndrome Correct Sickle-cell anemia Incorrect MCd135_6569
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'.
DiGeorge syndrome Incorrect Galactosemia Incorrect Triple X syndrome Incorrect Wolf-Hirschhorn syndrome Correct MCe6d9_d434
Which one of the following genetic disorders correspond to the description 'reduced hemoglobin proteins that result in variable outcomes including severe anemia'.
Beta-Thalassemia Correct Patau syndrome Incorrect Phenylketonuria Incorrect Tay-Sachs disease Incorrect MC864c_d815
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'.
Achondroplasia Incorrect Edwards syndrome Incorrect Huntington's disease Incorrect Phenylketonuria Correct MC2189_3615
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 15'.
Angelman syndrome Incorrect Cri du chat syndrome Incorrect Huntington's disease Incorrect Prader-Willi syndrome Correct MC153a_d908
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'.
Down syndrome Incorrect Klinefelter syndrome Incorrect Triple X syndrome Correct Wolf-Hirschhorn syndrome Incorrect MC1be3_db37
Which one of the following genetic disorders correspond to the description 'disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain'.
Cystic fibrosis Incorrect Huntington's disease Correct Maple syrup urine disease Incorrect Prader-Willi syndrome Incorrect MCfa21_233e
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'.
Hemophilia Incorrect Philadelphia chromosome Incorrect Tay-Sachs disease Incorrect WAGR syndrome Correct MCde90_e41c
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'.
Down syndrome Correct Galactosemia Incorrect Klinefelter syndrome Incorrect Patau syndrome Incorrect MC20b6_6971
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'.
Cri du chat syndrome Correct Fragile X syndrome Incorrect WAGR syndrome Incorrect Wolf-Hirschhorn syndrome Incorrect MC27e2_59fa
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'.
Down syndrome Incorrect Maple syrup urine disease Incorrect Patau syndrome Correct WAGR syndrome Incorrect MC539c_7177
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'.
DiGeorge syndrome Correct Down syndrome Incorrect Marfan syndrome Incorrect Triple X syndrome Incorrect MCe6a1_51e9
Which one of the following genetic disorders correspond to the description 'inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine'.
Cystic fibrosis Incorrect Phenylketonuria Correct Tay-Sachs disease Incorrect Triple X syndrome Incorrect MCb4f1_ed5c
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'.
Cystic fibrosis Incorrect Down syndrome Correct Edwards syndrome Incorrect Triple X syndrome Incorrect MCfdb0_63a9
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'.
Achondroplasia Incorrect Duchenne muscular dystrophy Incorrect Maple syrup urine disease Incorrect Philadelphia chromosome Correct MC217f_038b
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 22 is missing'.
Cri du chat syndrome Incorrect DiGeorge syndrome Correct Fragile X syndrome Incorrect Sickle-cell anemia Incorrect MC0bc2_9b2c
Which one of the following genetic disorders correspond to the description 'also known as monosomy X, includes a number of typical physical features observed such as webbed neck'.
Beta-Thalassemia Incorrect Hemophilia Incorrect Prader-Willi syndrome Incorrect Turner syndrome Correct MC44bb_9705
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'.
Cystic fibrosis Incorrect DiGeorge syndrome Incorrect Phenylketonuria Incorrect Tay-Sachs disease Correct MCf23c_455c
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'.
Cystic fibrosis Incorrect Duchenne muscular dystrophy Incorrect Huntington's disease Incorrect Prader-Willi syndrome Correct MC3c6e_7ae6
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 11 is missing'.
DiGeorge syndrome Incorrect Down syndrome Incorrect Marfan syndrome Incorrect WAGR syndrome Correct MC217f_539e
Which one of the following genetic disorders correspond to the description 'disorder caused when a small part of chromosome 22 is missing'.
Beta-Thalassemia Incorrect DiGeorge syndrome Correct Marfan syndrome Incorrect Tay-Sachs disease Incorrect MC8894_fb66
Which one of the following genetic disorders correspond to the description 'genetic metabolic disorder that increases the body's levels of phenylalanine'.
Beta-Thalassemia Incorrect DiGeorge syndrome Incorrect Galactosemia Incorrect Phenylketonuria Correct MC153a_421e
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'.
Down syndrome Incorrect Duchenne muscular dystrophy Incorrect Triple X syndrome Correct Wolf-Hirschhorn syndrome Incorrect MC5924_29bb
Which one of the following genetic disorders correspond to the description 'multi-systemic genetic disorder that affects the connective tissue'.
DiGeorge syndrome Incorrect Marfan syndrome Correct Patau syndrome Incorrect Turner syndrome Incorrect MCaff5_15e4
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'.
Marfan syndrome Correct Sickle-cell anemia Incorrect Tay-Sachs disease Incorrect WAGR syndrome Incorrect MC8894_f0f3
Which one of the following genetic disorders correspond to the description 'genetic metabolic disorder that increases the body's levels of phenylalanine'.
Maple syrup urine disease Incorrect Phenylketonuria Correct Philadelphia chromosome Incorrect Tay-Sachs disease Incorrect MC3ad4_3a7d
Which one of the following genetic disorders correspond to the description 'a genetic condition involving changes in part of the X chromosome'.
Angelman syndrome Incorrect Fragile X syndrome Correct Turner syndrome Incorrect WAGR syndrome Incorrect MC7f7a_f356
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'.
Down syndrome Incorrect Edwards syndrome Correct Huntington's disease Incorrect WAGR syndrome Incorrect MC7f7a_6c76
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'.
Beta-Thalassemia Incorrect Edwards syndrome Correct Prader-Willi syndrome Incorrect Tay-Sachs disease Incorrect MC28dc_9c37
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'.
Edwards syndrome Correct Hemophilia Incorrect Maple syrup urine disease Incorrect Sickle-cell anemia Incorrect MCde90_b2e6
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'.
Cystic fibrosis Incorrect Down syndrome Correct Hemophilia Incorrect WAGR syndrome Incorrect MC12c1_1030
Which one of the following genetic disorders correspond to the description 'metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly'.
Fragile X syndrome Incorrect Galactosemia Correct Huntington's disease Incorrect Wolf-Hirschhorn syndrome Incorrect MCf23c_e8b3
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'.
Down syndrome Incorrect Galactosemia Incorrect Huntington's disease Incorrect Prader-Willi syndrome Correct MC44bb_ecd5
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'.
Cri du chat syndrome Incorrect Fragile X syndrome Incorrect Tay-Sachs disease Correct WAGR syndrome Incorrect MCa584_99b1
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'.
Achondroplasia Incorrect Klinefelter syndrome Incorrect Phenylketonuria Incorrect WAGR syndrome Correct MCfdc3_6459
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'.
Angelman syndrome Correct Beta-Thalassemia Incorrect Edwards syndrome Incorrect Patau syndrome Incorrect MC12c1_a820
Which one of the following genetic disorders correspond to the description 'metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly'.
Galactosemia Correct Hemophilia Incorrect Patau syndrome Incorrect Prader-Willi syndrome Incorrect MCe716_042c
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'.
Achondroplasia Incorrect Edwards syndrome Correct Phenylketonuria Incorrect Philadelphia chromosome Incorrect MC20b6_9da6
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'.
Achondroplasia Incorrect Beta-Thalassemia Incorrect Cri du chat syndrome Correct Klinefelter syndrome Incorrect MCfcfd_207f
Which one of the following genetic disorders correspond to the description 'caused by duplications of the UBE3A gene located on chromosome 15'.
Angelman syndrome Correct Beta-Thalassemia Incorrect Patau syndrome Incorrect Sickle-cell anemia Incorrect MCf23c_955b
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'.
Fragile X syndrome Incorrect Maple syrup urine disease Incorrect Prader-Willi syndrome Correct Wolf-Hirschhorn syndrome Incorrect MCb129_5c88
Which one of the following genetic disorders correspond to the description 'an inherited bleeding disorder in which the blood does NOT clot properly'.
Beta-Thalassemia Incorrect DiGeorge syndrome Incorrect Duchenne muscular dystrophy Incorrect Hemophilia Correct MCaff5_3dfe
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'.
Cri du chat syndrome Incorrect Klinefelter syndrome Incorrect Marfan syndrome Correct WAGR syndrome Incorrect MC2596_eeee
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'.
Achondroplasia Correct Beta-Thalassemia Incorrect Cri du chat syndrome Incorrect Philadelphia chromosome Incorrect MC44bb_9d4a
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'.
Down syndrome Incorrect Phenylketonuria Incorrect Sickle-cell anemia Incorrect Tay-Sachs disease Correct MC35e7_b49e
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'.
Huntington's disease Incorrect Klinefelter syndrome Correct Patau syndrome Incorrect Prader-Willi syndrome Incorrect MCe716_c627
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'.
Edwards syndrome Correct Fragile X syndrome Incorrect Maple syrup urine disease Incorrect Triple X syndrome Incorrect MC35e7_fb5d
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'.
DiGeorge syndrome Incorrect Down syndrome Incorrect Klinefelter syndrome Correct Philadelphia chromosome Incorrect MC0ce9_69a4
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'.
Down syndrome Correct Phenylketonuria Incorrect Prader-Willi syndrome Incorrect Turner syndrome Incorrect MC8894_1bda
Which one of the following genetic disorders correspond to the description 'genetic metabolic disorder that increases the body's levels of phenylalanine'.
Phenylketonuria Correct Philadelphia chromosome Incorrect Turner syndrome Incorrect WAGR syndrome Incorrect MCd5e8_2a09
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'.
Cri du chat syndrome Incorrect Duchenne muscular dystrophy Incorrect Triple X syndrome Correct WAGR syndrome Incorrect MCada0_f37f
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 13th chromosome'.
Beta-Thalassemia Incorrect Duchenne muscular dystrophy Incorrect Edwards syndrome Incorrect Patau syndrome Correct MC1be3_6e23
Which one of the following genetic disorders correspond to the description 'disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain'.
Huntington's disease Correct Patau syndrome Incorrect WAGR syndrome Incorrect Wolf-Hirschhorn syndrome Incorrect MCada0_1bad
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 13th chromosome'.
Fragile X syndrome Incorrect Hemophilia Incorrect Patau syndrome Correct Sickle-cell anemia Incorrect MC5924_c9bc
Which one of the following genetic disorders correspond to the description 'multi-systemic genetic disorder that affects the connective tissue'.
Achondroplasia Incorrect Beta-Thalassemia Incorrect Huntington's disease Incorrect Marfan syndrome Correct MC898c_e8f2
Which one of the following genetic disorders correspond to the description 'autosomal recessive genetic disorder affecting most critically the lungs'.
Cri du chat syndrome Incorrect Cystic fibrosis Correct Fragile X syndrome Incorrect Phenylketonuria Incorrect MC2596_9073
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'.
Achondroplasia Correct Down syndrome Incorrect Duchenne muscular dystrophy Incorrect Patau syndrome Incorrect MCba7c_237a
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'.
Huntington's disease Incorrect Maple syrup urine disease Incorrect Sickle-cell anemia Incorrect Turner syndrome Correct MC27e2_bf9e
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'.
Edwards syndrome Incorrect Patau syndrome Correct Prader-Willi syndrome Incorrect Triple X syndrome Incorrect MC2189_d52d
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 15'.
Duchenne muscular dystrophy Incorrect Klinefelter syndrome Incorrect Patau syndrome Incorrect Prader-Willi syndrome Correct