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It depends on the context. If melanin was essential to good health, and a lack of it produces serious health problems then it could be considered a defect (assuming the lack of melanin was due to genetics). Having a total lack of it when the vast majority of creatures have it would certainly qualify as an unusual condition but just having less of it than others is a little too vague to be considered a defect without understanding the context. Like any 'trait' less of something may be beneficial in some environments but more of it may be beneficial in others. ----------------------------------- Albinism (complete or partial loss of melanin) is genetic.
What else can I help you with?
Is Klinefelter Syndrome sex-linked or autosomal?
Klinefelter Syndrome is sex-linked, because it is a genetic defect that results in a male having an extra X chromosome.
What does the term strain mean in relation with genetic crosses?
In genetic crosses, the term "strain" refers to a specific genetic line or variety of organisms that are pure-breeding for certain traits. Strains can differ in their genetic makeup and can be used in breeding experiments to study inheritance patterns and gene expression.
A trait such as having a crooked thumb is produced by a?
having a crooked thumb is produced by a combination of genetic factors and possibly environmental influences during development. This trait can be inherited from parents or arise from random genetic mutations.
Is genetic screening and genetic testing the same?
No, genetic screening and genetic testing are not the same. Genetic screening is used to identify individuals at risk for certain genetic conditions before symptoms appear, while genetic testing is used to diagnose or detect genetic mutations in individuals suspected of having a genetic condition.
What is the significance of having two sets of chromosomes in an organism's genetic makeup?
Having two sets of chromosomes in an organism's genetic makeup is significant because it allows for genetic diversity and stability. This redundancy helps in repairing damaged DNA, ensuring proper cell division, and providing a backup copy of genes. It also allows for genetic recombination during reproduction, leading to variation and adaptation in populations.
Has anyone heard of yorkies having scoliosis?
Any animal can be born with scoliosis. It's usually a genetic defect.
If the probability of a defect is 0.015 what is the probability of not having a defect?
1-.015 = .985
Defect on chromosome 21 where a third chromosome is present what is this defect called?
The defect of having a third chromosome 21 is known as Trisomy 21, which causes Down syndrome. This genetic condition leads to intellectual disabilities, characteristic facial features, and an increased risk of certain health issues.
What is another word for having a defect?
Defective
What does not perfect Having a defect mean?
it means peewee
What does defect mean?
adjective: having a defect or flaw;flaulty;imperfect or characterized by subnormal intelligence;behavior noun:a defective person or thing
Cold shortness in steel?
The steel having this defect cracks when being worked in cold state. This defect is due to presence of excess of phosphorus
Are babies cute?
Yes.... when they'rye not crying, or having a birth defect.
Is having bird chest a birth defect?
No, having a "bird chest," often referred to as pectus excavatum, is not classified as a birth defect but rather a chest wall deformity that can occur during development. It involves a sunken appearance of the breastbone and can vary in severity. While it is typically present at birth, its exact cause is not well understood, and it may be associated with genetic factors. In some cases, it can affect physical health or self-esteem, leading individuals to seek treatment.
Is having two arms considered an inherited trait?
Yes, having two arms is considered an inherited trait, as it is a characteristic determined by the genetic information passed down from parents to offspring. The presence of two arms is part of the normal human anatomy, which is encoded in our DNA. However, variations can occur due to genetic mutations or developmental issues, but these are exceptions rather than the norm.
Which are the two organelles having their own genetic material. What is their significance?
Nucleus & Mitochondria are the two organelles having their own genetic material.
Can thalassemia develop at the age of 20 years?
Very unlikely. Thalassemia is an inherited disease, affected persons are born with the genetic disorders. However, silent carriers (Alpha Thalassemia, 1 gene defect) or Beta Thalassemia Trait (1 gene defect), do not have significiant symptoms. Consequently, if this person did not have any relevant blood tests till the age of 20, he/she might no be aware of having the condition. That's only a hypothetical suggestion.
