9fb0_07a3
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs Cri du chat syndrome usually include a high-pitched cat-like cry, mental disability, delayed development, distinctive facial features, widely-spaced eyes Patau syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 13 Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain MAT9fb0_09ca
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Down syndrome chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 21st chromosome Maple syrup urine disease metabolic disorder affecting branched-chain amino acids Wolf-Hirschhorn syndrome disorder caused when a small part of chromosome 4 is missing Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull MAT9fb0_0b70
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing Edwards syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 18 Turner syndrome a condition that affects only females, results when one of their X chromosomes is missing or partially missing Phenylketonuria genetic metabolic disorder that increases the body's levels of phenylalanine MAT9fb0_0eb5
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Prader-Willi syndrome a genetic disorder caused by a loss of function of specific genes on chromosome 15 Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Maple syrup urine disease gets its name from the distinctive sweet odor of affected infants' urine MAT9fb0_129b
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Cri du chat syndrome usually include a high-pitched cat-like cry, mental disability, delayed development, distinctive facial features, widely-spaced eyes Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs Turner syndrome also known as monosomy X, includes a number of typical physical features observed such as webbed neck Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Angelman syndrome disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15 MAT9fb0_13ba
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Cri du chat syndrome usually include a high-pitched cat-like cry, mental disability, delayed development, distinctive facial features, widely-spaced eyes Triple X syndrome a genetic condition in females which there are three copies of the X chromosome Edwards syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 18 MAT9fb0_1400
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing Cystic fibrosis a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Maple syrup urine disease metabolic disorder affecting branched-chain amino acids MAT9fb0_17c2
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Edwards syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 18 Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Fragile X syndrome a genetic condition involving changes in part of the X chromosome Cystic fibrosis a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat MAT9fb0_18e8
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Maple syrup urine disease gets its name from the distinctive sweet odor of affected infants' urine Turner syndrome a condition that affects only females, results when one of their X chromosomes is missing or partially missing DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 MAT9fb0_1f2a
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Maple syrup urine disease metabolic disorder affecting branched-chain amino acids Patau syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13 Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly DiGeorge syndrome disorder caused when a small part of chromosome 22 is missing Phenylketonuria inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine MAT9fb0_1fff
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Tay-Sachs disease a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Fragile X syndrome a genetic condition involving changes in part of the X chromosome Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 MAT9fb0_21fe
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Prader-Willi syndrome a genetic disorder caused by a loss of function of specific genes on chromosome 15 Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Patau syndrome chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 13th chromosome MAT9fb0_2262
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Patau syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13 Down syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21 Klinefelter syndrome also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome MAT9fb0_2480
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Cystic fibrosis a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Down syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21 Fragile X syndrome a genetic condition involving changes in part of the X chromosome Wolf-Hirschhorn syndrome disorder caused when a small part of chromosome 4 is missing MAT9fb0_2590
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs Down syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21 Tay-Sachs disease people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_25d1
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Patau syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 13 DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Phenylketonuria genetic metabolic disorder that increases the body's levels of phenylalanine Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly MAT9fb0_2835
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Patau syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 13 Turner syndrome a condition that affects only females, results when one of their X chromosomes is missing or partially missing Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 Triple X syndrome a genetic condition in females which there are three copies of the X chromosome MAT9fb0_2887
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Wolf-Hirschhorn syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 4 Turner syndrome a condition that affects only females, results when one of their X chromosomes is missing or partially missing Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 MAT9fb0_29a5
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Wolf-Hirschhorn syndrome caused by a deletion within HSA band on the short arm of chromosome 4 Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Tay-Sachs disease people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase Turner syndrome a condition that affects only females, results when one of their X chromosomes is missing or partially missing MAT9fb0_29c8
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Klinefelter syndrome also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome Maple syrup urine disease gets its name from the distinctive sweet odor of affected infants' urine Wolf-Hirschhorn syndrome caused by a deletion within HSA band on the short arm of chromosome 4 Patau syndrome result of a random error that causes a person to be born with an extra chromosome 13 Fragile X syndrome a genetic condition involving changes in part of the X chromosome MAT9fb0_2a04
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Marfan syndrome multi-systemic genetic disorder that affects the connective tissue WAGR syndrome disorder caused when a small part of chromosome 11 is missing Wolf-Hirschhorn syndrome caused by a deletion within HSA band on the short arm of chromosome 4 Down syndrome result of a random error that causes a person to be born with an extra chromosome 21 MAT9fb0_2cb6
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Angelman syndrome disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15 Down syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21 Philadelphia chromosome cancerous chromosomal abnormality that is manifested as a shortened version of human chromosome 22 MAT9fb0_2d73
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Fragile X syndrome a genetic condition involving changes in part of the X chromosome Patau syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13 Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing Cystic fibrosis a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_2ea0
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Down syndrome chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 21st chromosome Wolf-Hirschhorn syndrome genetic condition caused by a deletion of a group of genes located on chromosome number 4 Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly MAT9fb0_330e
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_33c2
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Tay-Sachs disease people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase MAT9fb0_393c
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Tay-Sachs disease a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord Cri du chat syndrome usually include a high-pitched cat-like cry, mental disability, delayed development, distinctive facial features, widely-spaced eyes Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Maple syrup urine disease metabolic disorder affecting branched-chain amino acids Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells MAT9fb0_3aea
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Phenylketonuria genetic metabolic disorder that increases the body's levels of phenylalanine Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain MAT9fb0_3cb3
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome WAGR syndrome disorder caused when a small part of chromosome 11 is missing Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull MAT9fb0_3f23
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Turner syndrome also known as monosomy X, includes a number of typical physical features observed such as webbed neck Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly MAT9fb0_4128
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain Fragile X syndrome a genetic condition involving changes in part of the X chromosome Turner syndrome a condition that affects only females, results when one of their X chromosomes is missing or partially missing DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 MAT9fb0_43a1
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Tay-Sachs disease a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull MAT9fb0_43d8
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Fragile X syndrome a genetic condition involving changes in part of the X chromosome Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes Patau syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13 Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 MAT9fb0_45de
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Marfan syndrome multi-systemic genetic disorder that affects the connective tissue Angelman syndrome disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15 WAGR syndrome genetic condition caused by a deletion of a group of genes located on chromosome number 11 Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_4800
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Fragile X syndrome a genetic condition involving changes in part of the X chromosome Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_497b
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Turner syndrome a condition that affects only females, results when one of their X chromosomes is missing or partially missing Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Maple syrup urine disease metabolic disorder affecting branched-chain amino acids Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_4bc7
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Patau syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 13 Edwards syndrome chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 18th chromosome Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Fragile X syndrome a genetic condition involving changes in part of the X chromosome Wolf-Hirschhorn syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 4 MAT9fb0_4d8a
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Fragile X syndrome a genetic condition involving changes in part of the X chromosome Prader-Willi syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 15 WAGR syndrome disorder caused when a small part of chromosome 11 is missing Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull MAT9fb0_5084
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Klinefelter syndrome also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Edwards syndrome result of a random error that causes a person to be born with an extra chromosome 18 Angelman syndrome disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15 MAT9fb0_530a
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Patau syndrome chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 13th chromosome Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time DiGeorge syndrome disorder caused when a small part of chromosome 22 is missing Edwards syndrome result of a random error that causes a person to be born with an extra chromosome 18 Triple X syndrome a genetic condition in females which there are three copies of the X chromosome MAT9fb0_5590
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Edwards syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 18 Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain MAT9fb0_579c
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Angelman syndrome disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15 WAGR syndrome genetic condition caused by a deletion of a group of genes located on chromosome number 11 Tay-Sachs disease a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_5afe
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Philadelphia chromosome cancerous chromosomal abnormality that is manifested as a shortened version of human chromosome 22 Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Maple syrup urine disease metabolic disorder affecting branched-chain amino acids WAGR syndrome disorder caused when a small part of chromosome 11 is missing Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly MAT9fb0_5c05
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 Marfan syndrome multi-systemic genetic disorder that affects the connective tissue DiGeorge syndrome disorder caused when a small part of chromosome 22 is missing Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull MAT9fb0_5ed6
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Edwards syndrome result of a random error that causes a person to be born with an extra chromosome 18 Prader-Willi syndrome a genetic disorder caused by a loss of function of specific genes on chromosome 15 WAGR syndrome disorder caused when a small part of chromosome 11 is missing Triple X syndrome a genetic condition in females which there are three copies of the X chromosome Turner syndrome also known as monosomy X, includes a number of typical physical features observed such as webbed neck MAT9fb0_6460
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Maple syrup urine disease metabolic disorder affecting branched-chain amino acids Wolf-Hirschhorn syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 4 Down syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 21 Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs Phenylketonuria inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine MAT9fb0_65a0
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Fragile X syndrome a genetic condition involving changes in part of the X chromosome Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing WAGR syndrome genetic condition caused by a deletion of a group of genes located on chromosome number 11 Prader-Willi syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 15 Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain MAT9fb0_69bf
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Fragile X syndrome a genetic condition involving changes in part of the X chromosome Patau syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 13 Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Triple X syndrome also known as 47,XXX, is a genetic disorder that results in a female that has three X chromosomes Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_6f6a
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Philadelphia chromosome cancerous chromosomal abnormality that is manifested as a shortened version of human chromosome 22 Prader-Willi syndrome a genetic disorder caused by a loss of function of specific genes on chromosome 15 Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Patau syndrome chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 13th chromosome Down syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21 MAT9fb0_726b
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Philadelphia chromosome cancerous chromosomal abnormality that is manifested as a shortened version of human chromosome 22 DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain Fragile X syndrome a genetic condition involving changes in part of the X chromosome MAT9fb0_7413
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
WAGR syndrome disorder caused when a small part of chromosome 11 is missing Cystic fibrosis a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Angelman syndrome disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15 Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells MAT9fb0_7555
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
WAGR syndrome disorder caused when a small part of chromosome 11 is missing Maple syrup urine disease gets its name from the distinctive sweet odor of affected infants' urine Tay-Sachs disease a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord Wolf-Hirschhorn syndrome caused by a deletion within HSA band on the short arm of chromosome 4 Triple X syndrome a genetic condition in females which there are three copies of the X chromosome MAT9fb0_776a
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Down syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 21 Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly MAT9fb0_867e
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Maple syrup urine disease gets its name from the distinctive sweet odor of affected infants' urine Fragile X syndrome a genetic condition involving changes in part of the X chromosome Patau syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13 Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain Philadelphia chromosome cancerous chromosomal abnormality that is manifested as a shortened version of human chromosome 22 MAT9fb0_8ba6
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Edwards syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 18 Cri du chat syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 5 WAGR syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 11 Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Down syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 21 MAT9fb0_96c3
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Wolf-Hirschhorn syndrome disorder caused when a small part of chromosome 4 is missing WAGR syndrome disorder caused when a small part of chromosome 11 is missing Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Fragile X syndrome a genetic condition involving changes in part of the X chromosome MAT9fb0_986a
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Maple syrup urine disease gets its name from the distinctive sweet odor of affected infants' urine Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Edwards syndrome result of a random error that causes a person to be born with an extra chromosome 18 Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_9979
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Wolf-Hirschhorn syndrome caused by a deletion within HSA band on the short arm of chromosome 4 Edwards syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 18 Marfan syndrome multi-systemic genetic disorder that affects the connective tissue MAT9fb0_9999
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Angelman syndrome disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15 Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing Wolf-Hirschhorn syndrome genetic condition caused by a deletion of a group of genes located on chromosome number 4 MAT9fb0_9b6d
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Cri du chat syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 5 Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Cystic fibrosis a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull MAT9fb0_9b6d
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Patau syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13 Fragile X syndrome a genetic condition involving changes in part of the X chromosome Prader-Willi syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 15 Phenylketonuria inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine DiGeorge syndrome disorder caused when a small part of chromosome 22 is missing MAT9fb0_a068
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Edwards syndrome result of a random error that causes a person to be born with an extra chromosome 18 Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Prader-Willi syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 15 Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly MAT9fb0_ab56
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Edwards syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 18 Wolf-Hirschhorn syndrome caused by a deletion within HSA band on the short arm of chromosome 4 Prader-Willi syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 15 Turner syndrome a condition that affects only females, results when one of their X chromosomes is missing or partially missing Tay-Sachs disease people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase MAT9fb0_accd
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 Maple syrup urine disease metabolic disorder affecting branched-chain amino acids Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Wolf-Hirschhorn syndrome disorder caused when a small part of chromosome 4 is missing Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing MAT9fb0_ad6d
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
WAGR syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 11 Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes Philadelphia chromosome cancerous chromosomal abnormality that is manifested as a shortened version of human chromosome 22 Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing MAT9fb0_aebb
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Down syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21 Edwards syndrome result of a random error that causes a person to be born with an extra chromosome 18 Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome Marfan syndrome multi-systemic genetic disorder that affects the connective tissue Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_b05b
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Turner syndrome also known as monosomy X, includes a number of typical physical features observed such as webbed neck Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain Maple syrup urine disease metabolic disorder affecting branched-chain amino acids Prader-Willi syndrome a genetic disorder caused by a loss of function of specific genes on chromosome 15 MAT9fb0_b4d1
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs Phenylketonuria inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Wolf-Hirschhorn syndrome caused by a deletion within HSA band on the short arm of chromosome 4 Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_b99e
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Philadelphia chromosome cancerous chromosomal abnormality that is manifested as a shortened version of human chromosome 22 Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome WAGR syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 11 Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Triple X syndrome a genetic condition in females which there are three copies of the X chromosome MAT9fb0_b9a6
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Fragile X syndrome a genetic condition involving changes in part of the X chromosome Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs MAT9fb0_b9d2
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Triple X syndrome also known as 47,XXX, is a genetic disorder that results in a female that has three X chromosomes Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Cri du chat syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 5 WAGR syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 11 Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome MAT9fb0_baf7
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Edwards syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 18 Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Cystic fibrosis a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes MAT9fb0_bca6
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Turner syndrome also known as monosomy X, includes a number of typical physical features observed such as webbed neck Down syndrome chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 21st chromosome MAT9fb0_c085
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Maple syrup urine disease metabolic disorder affecting branched-chain amino acids Wolf-Hirschhorn syndrome disorder caused when a small part of chromosome 4 is missing Klinefelter syndrome also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome Down syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 21 MAT9fb0_c152
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Down syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 21 Fragile X syndrome a genetic condition involving changes in part of the X chromosome DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_c343
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Tay-Sachs disease people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Klinefelter syndrome also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes MAT9fb0_c48f
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Tay-Sachs disease people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase Maple syrup urine disease metabolic disorder affecting branched-chain amino acids Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Wolf-Hirschhorn syndrome disorder caused when a small part of chromosome 4 is missing Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly MAT9fb0_c88c
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Edwards syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 18 Maple syrup urine disease gets its name from the distinctive sweet odor of affected infants' urine DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Patau syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 13 Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia MAT9fb0_cff5
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs Down syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 21 Cri du chat syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 5 Phenylketonuria inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time MAT9fb0_d05b
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Edwards syndrome chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 18th chromosome Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly DiGeorge syndrome disorder caused when a small part of chromosome 22 is missing Tay-Sachs disease people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase MAT9fb0_d2c7
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Cystic fibrosis autosomal recessive genetic disorder affecting most critically the lungs Fragile X syndrome a genetic condition involving changes in part of the X chromosome Cri du chat syndrome usually include a high-pitched cat-like cry, mental disability, delayed development, distinctive facial features, widely-spaced eyes Patau syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 13 MAT9fb0_d508
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Edwards syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 18 Cystic fibrosis a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat Fragile X syndrome a genetic condition involving changes in part of the X chromosome Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes Triple X syndrome a genetic condition in females which there are three copies of the X chromosome MAT9fb0_db60
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Marfan syndrome individuals with the condition tend to be tall and thin, with long arms, legs, fingers, and toes Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing MAT9fb0_dba4
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Phenylketonuria genetic metabolic disorder that increases the body's levels of phenylalanine Triple X syndrome also known as 47,XXX, is a genetic disorder that results in a female that has three X chromosomes Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 MAT9fb0_dd88
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Phenylketonuria genetic metabolic disorder that increases the body's levels of phenylalanine Patau syndrome result of a random error that causes a person to be born with an extra chromosome 13 WAGR syndrome genetic condition caused by a deletion of a group of genes located on chromosome number 11 Triple X syndrome a genetic condition in females which there are three copies of the X chromosome MAT9fb0_de20
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Klinefelter syndrome also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome Tay-Sachs disease a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord DiGeorge syndrome disorder caused when a small part of chromosome 22 is missing Wolf-Hirschhorn syndrome disorder caused when a small part of chromosome 4 is missing Patau syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 13 MAT9fb0_e907
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Philadelphia chromosome cancerous chromosomal abnormality that is manifested as a shortened version of human chromosome 22 Cystic fibrosis a faulty protein that affects the cells, tissues, and the glands that make mucus and sweat Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time MAT9fb0_ecf8
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Turner syndrome a condition that affects only females, results when one of their X chromosomes is missing or partially missing DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Marfan syndrome multi-systemic genetic disorder that affects the connective tissue MAT9fb0_eea1
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Triple X syndrome a genetic condition in females which there are three copies of the X chromosome Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Cri du chat syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 5 Sickle-cell anemia affects your red blood cells, turning them from round flexible discs into stiff and sticky, long, and rigid cells Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material MAT9fb0_eec3
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Wolf-Hirschhorn syndrome disorder caused when a small part of chromosome 4 is missing Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 Patau syndrome chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 13th chromosome MAT9fb0_f1b3
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Edwards syndrome result of a random error that causes a person to be born with an extra chromosome 18 Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Klinefelter syndrome also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome Cri du chat syndrome usually include a high-pitched cat-like cry, mental disability, delayed development, distinctive facial features, widely-spaced eyes Duchenne muscular dystrophy disorder that affects the muscles, leading to muscle wasting that gets worse over time MAT9fb0_f415
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 Cri du chat syndrome disorder caused when a small part of chromosome 5 is missing Tay-Sachs disease people with the disorder do NOT have enough of an enzyme called beta-hexosaminidase Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly MAT9fb0_f72e
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Maple syrup urine disease gets its name from the distinctive sweet odor of affected infants' urine DiGeorge syndrome disorder caused when a small part of chromosome 22 is missing Angelman syndrome disorder that is due to a extra piece (duplication) of a specific gene on chromosome 15 MAT9fb0_f83f
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Patau syndrome a chromosomal abnormality, in which the cells of the body contain extra genetic material from chromosome 13 Phenylketonuria inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull WAGR syndrome genetic condition caused by a deletion of a group of genes located on chromosome number 11 Fragile X syndrome a genetic condition involving changes in part of the X chromosome MAT9fb0_f870
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Klinefelter syndrome also known as 47,XXY, is a syndrome where a male has an additional copy of the X chromosome Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Huntington's disease disorder that causes the progressive breakdown (degeneration) of nerve cells in the brain Tay-Sachs disease a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord MAT9fb0_fa2a
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 Philadelphia chromosome forms when chromosome 9 and chromosome 22 break and exchange portions of their genetic material Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome DiGeorge syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 22 WAGR syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 11 MAT9fb0_fd56
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Marfan syndrome multi-systemic genetic disorder that affects the connective tissue Edwards syndrome genetic disorder caused by the presence of all or part of a third copy of chromosome 18 Phenylketonuria inherited disorder that causes an amino acid called phenylalanine to build up in the body Angelman syndrome caused by duplications of the UBE3A gene located on chromosome 15 DiGeorge syndrome disorder caused when a small part of chromosome 22 is missing MAT9fb0_fdcf
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Fragile X syndrome a genetic condition involving changes in part of the X chromosome Beta-Thalassemia reduced hemoglobin proteins that result in variable outcomes including severe anemia Prader-Willi syndrome disorder that is due to a missing piece (deletion) of a specific part of chromosome 15 Hemophilia an inherited bleeding disorder in which the blood does NOT clot properly Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome MAT9fb0_fe20
Match each of the following genetic disorders with their corresponding descriptions.
Note: Each choice will be used exactly once.
Galactosemia metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly Triple X syndrome also known as 47,XXX, is a genetic disorder that results in a female that has three X chromosomes Wolf-Hirschhorn syndrome genetic condition caused by a deletion of a group of genes located on chromosome number 4 Klinefelter syndrome result of a random error that causes a male to be born with an extra X chromosome Achondroplasia impairs the growth of bone in the limbs and causes abnormal growth in the spine and skull