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Recessive disorder that results from the absence of an enzyme that converts one amino acid into another one?
Phenylketonuria (PKU) is a recessive disorder caused by the absence of the enzyme phenylalanine hydroxylase, which converts phenylalanine to tyrosine. This leads to a buildup of phenylalanine in the body, causing intellectual disability and other complications if not managed through a restricted diet.
A person who has inherited the autosomal recessive disorder called?
A person who has inherited an autosomal recessive disorder will have two copies of the mutated gene, one from each parent. This results in the individual expressing the disorder. Symptoms can vary depending on the specific disorder.
Who does a male inherit an autosomal recessive disorder from?
A male can inherit an autosomal recessive disorder from both of his carrier parents, who each pass down a copy of the mutated gene. This results in the male having two copies of the mutated gene, leading to the manifestation of the disorder.
Is CF X-linked or incomplete dominance?
Cystic fibrosis (CF) is an autosomal recessive disorder, not an X-linked disorder. It means that both copies of the gene responsible for CF need to be mutated in order to develop the disorder. Incomplete dominance refers to a genetic trait where the heterozygous condition results in an intermediate phenotype, which is not the case for CF.
Is an x-linked recessive bleeding disorder caused by a missing coagulation factor?
Yes, the disorder you are referring to is hemophilia A, which is caused by a deficiency or missing factor VIII in the blood. This results in impaired blood clotting and leads to prolonged bleeding after injury or surgery. It is inherited in an X-linked recessive pattern, meaning it predominantly affects males.
Recessive disorder that results from the absence of an enzyme that converts one amino acid into another one?
Phenylketonuria (PKU) is a recessive disorder caused by the absence of the enzyme phenylalanine hydroxylase, which converts phenylalanine to tyrosine. This leads to a buildup of phenylalanine in the body, causing intellectual disability and other complications if not managed through a restricted diet.
A person who has inherited the autosomal recessive disorder called?
A person who has inherited an autosomal recessive disorder will have two copies of the mutated gene, one from each parent. This results in the individual expressing the disorder. Symptoms can vary depending on the specific disorder.
Who does a male inherit an autosomal recessive disorder from?
A male can inherit an autosomal recessive disorder from both of his carrier parents, who each pass down a copy of the mutated gene. This results in the male having two copies of the mutated gene, leading to the manifestation of the disorder.
Is CF X-linked or incomplete dominance?
Cystic fibrosis (CF) is an autosomal recessive disorder, not an X-linked disorder. It means that both copies of the gene responsible for CF need to be mutated in order to develop the disorder. Incomplete dominance refers to a genetic trait where the heterozygous condition results in an intermediate phenotype, which is not the case for CF.
Is an x-linked recessive bleeding disorder caused by a missing coagulation factor?
Yes, the disorder you are referring to is hemophilia A, which is caused by a deficiency or missing factor VIII in the blood. This results in impaired blood clotting and leads to prolonged bleeding after injury or surgery. It is inherited in an X-linked recessive pattern, meaning it predominantly affects males.
Is progeria a dominant or recessive gene?
progeria is recessive, that's an easy question, dont be dumbactually progeria is dominant, according to the Progeria Research Foundation
What is the difference between genetic a disorder and a genetic mutation?
Mutation is any change in the genetic code of an individual regardless of how the change manifests. A genetic disorder is the result of an unfavorable mutation that results through through heterozygous recessive parents producing a homozygous recessive offspring, a random dominant mutation, or multiple polygenic mutations that compound for a negative effect on an individual as examples.
What does homo recessive mean?
"Homozygous recessive" means having two copies of a recessive allele for a particular gene. This usually results in the expression of the recessive trait.
Is Tay-Sach Disease sex-linked dominate or recessive?
Tay-Sachs disease is caused by a genetic mutation in the HEXA gene on (human) chromosome 15. It is is a rare autosomal recessive genetic disorder and not sex-linked.Two Tay-Sachs alleles are required for an individual to exhibit symptoms of the disease.It causes a progressive deterioration of nerve cells and of mental and physical abilities that begins around six months of age and usually results in death by the age of four.
Which genotype will give rise to the Bombay phenotype?
The Bombay phenotype is caused by a homozygous recessive mutation in the FUT1 gene, which results in the absence of H antigen on red blood cells. Therefore, the genotype for the Bombay phenotype is hh.
What genetic condition results in the trait indicated by the blue color being expressed in the individuals shown here?
The genetic condition is called Oculocutaneous Albinism, which results in the lack of pigmentation in the eyes, skin, and hair. This leads to a lighter or bluish color in the eyes due to the absence of melanin.
What is the difference between a genetic disorder and a genetic mutation?
A genetic disorder is something an individual is born with, and results from a problem within their genetic material. This means they have inherited the disease or disorder from their Mother or Father. You cannot inherit an infectious disease, you acquire it during your lifetime from a germ, such as a virus or a bacterium. You can also recover from an infectious disease, whereas you will always suffer from a genetic disorder if you inherit one.
