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females
Mossie Lueilwitz
Both males and females can be carriers of autosomal disorders. However, autosomal disorders are typically recessive, meaning that an individual usually needs to inherit two copies of the mutated gene (one from each parent) to develop the disorder. Carriers have only one copy of the mutated gene and do not display symptoms themselves, but can pass the gene on to their children.
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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.
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.
How is carrier different from a person that has a disorder?
The carrier typically remains unaffected by the disorder.
Is the maple syrup disease sex-linked?
Yes, maple syrup urine disease (MSUD) is an autosomal recessive genetic disorder, not a sex-linked disorder. It is caused by mutations in genes on autosomal chromosomes, which both males and females can inherit equally.
Cystic fibrosis autosomal dominant?
Cystic fibrosis is an autosomal recessive genetic disorder caused by mutations in the CFTR gene. It is not an autosomal dominant condition. Individuals need to inherit two copies of the mutated gene (one from each parent) to have the 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 suicidal behavior autosomal disorder?
well, technically, suicidal behavior can be triggered by almost anything. Autosomal disorders very rarely have anything to do with behavior. but, im confused by the way you worded your question. Is it ,"Is suicdal behavior an autosomal disorder?" or "Can suicidal behavior be caused by an autosomal disorder?"
Is huntington disease an autosomal disorder?
Yes. HD is a disease of autosomal dominant inheritance.
Which of these is in autosomal recessive disorder?
You did not list a "these" to chose from.
Is cystic fibrosis a dominant or co-dominant disorder?
It is autosomal recessive and it is not a disorder! Cystic Fibrosis is a disease.
What is the genotype of a person who is a carrier of a autosomal recessive trait?
The genotype of a person who is a carrier of an autosomal recessive trait is typically heterozygous, meaning they carry one copy of the recessive allele and one copy of the dominant allele for that trait. This would be represented as Aa, with the lowercase "a" representing the recessive allele.
What type of genetic disease is Refsum?
Refsum disease is inherited as an autosomal recessive disorder, which means that two unaffected carrier parents have a 25% chance of having an affected child in every pregnancy.
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.
How is carrier different from a person that has a disorder?
The carrier typically remains unaffected by the disorder.
What category of genetic disorder is huntingtons disease?
Autosomal Dominant
Is Polydactyly autosomal or sex-linked?
Polydactyly is typically autosomal, meaning it is not linked to the sex chromosomes. However, in some rare cases, polydactyly can be part of a sex-linked genetic disorder.
Is alkaptonuria caused by a recessive or dominant allele?
Alkaptonuria is caused by a recessive allele. It is an autosomal recessive disorder, meaning that an individual needs to inherit two copies of the defective gene (one from each parent) in order to have the condition.
