1) Symptoms of 4 disorders are listed. Using the lists given, fill in the correct letter for the condition name and inheritance type. Letters may be used more than once. Symptoms Condition Inheritance Туре Loss of muscle control and decline in mental ability Shades of red and green are hard to distinguish Lack of skin pigmentation Cannot produce one of the necessary blood clotting factors Conditions: Inheritance Type: A: Albinism E: X-linked dominant B: Huntington Disease F: X-linked recessive G: Y-linked C: Hemophilia H: Autosomal dominant I: Autosomal recessive D: CVD

1) Symptoms of 4 disorders are listed. Using the lists given, fill in the correct letter for the condition name and inheritance type. Letters may be used more than once. Symptoms Condition Inheritance Туре Loss of muscle control and decline in mental ability Shades of red and green are hard to distinguish Lack of skin pigmentation Cannot produce one of the necessary blood clotting factors Conditions: Inheritance Type: A: Albinism E: X-linked dominant B: Huntington Disease F: X-linked recessive G: Y-linked C: Hemophilia H: Autosomal dominant I: Autosomal recessive D: CVD

Name: 1) Symptoms of 4 disorders are listed. Using the lists given, fill in
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Description: 1) Symptoms of 4 disorders are listed. Using the lists given, fill in the correct letter for thecondition name and inheritance type. Letters may be used more than once.SymptomsConditionInheritanceТуреLoss of muscle control and decline in mental abil

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter11: Genome Alterations: Mutation And Epigenetics

Section: Chapter Questions

Problem 5QP: Achondroplasia is a rare dominant autosomal defect resulting in dwarfism. The unaffected brother of...

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Pseudohypertrophic muscular dystrophy is an inheriteddisorder that causes gradual deterioration of the muscles. It isseen almost exclusively in boys born to apparently unaffectedparents and usually results in death in the early teens. Isthis disorder caused by a dominant or a recessive allele?Is its inheritance sex-linked or autosomal? How do youknow? Explain why this disorder is almost never seen in girls.
Unattached earlobes (E) are dominant over attached earlobes (e) [Figure (a) and (b)]. If a woman with unattached earlobes and a man with attached earlobes have children, what percentage of their children has the possibility of having unattached earlobes if the mother is homozygous for the trait?
Almond-shaped (E) eyes is dominant over round eyes. Presence of freckles (F) is also a dominant trait. Medium-sized nose, however, may be inherited if one parent has a large (L) nose and the other has a small (S) nose. Achondroplasia (A) is an autosomal dominant disorder that leads to dwarfism but not lethal.A woman homozygous for normal height, with freckles, almond-shaped eyes, small nose, and Type A blood, has a Type O mother with no freckles and a type AB father with round eyes. She is engaged to a man with achondroplasia, round eyes and medium sized nose. Unlike his father, his mother is of normal height. Both his parents have Type O blood but nobody from both sides of his family has or had freckles. -Write the COMPLETE genotypes of the man and the woman. Clearly indicate which genotype belongs to whom Based on their genotypes, what is the probability that they will have: -4 a daughter with round eyes, freckles, and medium sized nose?-6 a daughter with same genotype as the…
Almond-shaped (E) eyes is dominant over round eyes. Presence of freckles (F) is also a dominant trait. Medium-sized nose, however, may be inherited if one parent has a large (L) nose and the other has a small (S) nose. Achondroplasia (A) is an autosomal dominant disorder that leads to dwarfism but not lethal.A woman homozygous for normal height, with freckles, almond-shaped eyes, small nose, and Type A blood, has a Type O mother with no freckles and a type AB father with round eyes. She is engaged to a man with achondroplasia, round eyes and medium sized nose. Unlike his father, hismother is of normal height. Both his parents have Type O blood but nobody from both sides of his family has or had freckles. 1.What is the complete genotypes of the man and the woman. Clearly indicate which genotype belongs to whom? 2.Based on their genotypes, what is the probability that they will have:- a child with Achondroplasia?- a child of normal height?- a child with type AB blood?
Cystic fibrosis is determined by simple dominant-recessive inheritance, where the trait for cystic fibrosis is recessive. Given Rnormal, r is CF gene, complete the following Punnett square
Albinism is a recessive autosomal trait for skin pigmentation. Hemophilia is a sex-linked recessivedisorder of the blood. assign alleles to the traitsA – normal skin pigmentation X H – normal blooda – albino X h - hemophilia A double heterozygous woman marries a non-hemophilic man and heterozygous for skinpigmentation.  Double heterozygous means heterozygous for both traits. Aa for skin pigmentation andX H X h for blood trait. Therefore, the genotype of the woman is AaX H X h .  Non-hemophilic man is X H Y and heterozygous for skin pigmentation is Aa. The genotype,therefore, of the man is AaX H Y. What is the probability that they will have:a. a child with normal skin? _____________________b. a child with normal blood? _____________________c. an albino girl? _____________________d. A hemophilic boy? _____________________
Johnny has unattached earlobes (a dominant trait) like his father, but his mother has attached earlobes. What is johnny’s genotype?
Cystic fibrosis is chracterized by: 1) Heterozygous expression of an autosomal recessive trait 2) Elevated sweat chloride levels 3) Pancreatic obstruction 4) All of these are correct
If a child has type O blood and the mother is type A, then which ofthe following might be the blood type of the child’s father?a. A onlyb. A or Oc. B onlyd. A, B, or Oe. O only
In individuals affected by cystic fibrosis, salt crystals may appear afterperspiration dries up. In addition, the disease causes respiratory disorderswhich can be both debilitating and lethal. It occurs in individuals homozygousfor the recessive gene. Two normal parents had a daughter with thesymptoms of this disease, and a normal son who marries a normal womanwith an afflicted A test (salt concentration in perspiration of heterozygotes ishigher than normal) disclosed that both are indeed carriers of the gene. If thefirst child born to the mating in (b) was defective, what is the probability thatthe 2nd child would also be defective?Express answer in fraction form
In humans, normal skin color (A) is dominant over albino (a). An albino man marries a normal woman whose mother was an albino and whose father has normal skin color. What is the genotype of the man and the woman? What proportion of their children would be expected to be both normal skin pigmentation and have the trait for albino?
B- Whattype of genetic inheritance determinesthe ABO blood group system?