Wiki User
∙ 12y agoFirst of all, it important to understand that the male chromosome (the Y chromosome) basically only contains the genetic material that is required to make someone male. There isn't room on it for much more. So, the sex linked disorder genes are usually only present on the X chromosome. These genes are also usually recessive traits. So, they only manifest themselves when there is not a dominant gene of the same type to override them. This will most often happen in a male where they will only have one copy of the gene on the X chromosome. Thus, traits like red-green color blindness that are carried by the X chromosome usually only manifest themselves in the male offspring of the parents and they will receive them from their mothers. Females can only inherit these traits if they are passed on by both parents. In this case, the father WILL have the trait and the mother will be a carrier at the very least.
Wiki User
∙ 12y agoIt depends on the specific information given in the pedigree. If the father has the disorder allele on his X chromosome, he would be affected. If he does not carry the disorder allele, he would not be affected. The father's status would need to be determined based on the information provided in the pedigree.
Blindness is typically considered a disability or impairment rather than a disease or disorder. It can be caused by a variety of factors such as injury, genetic conditions, or certain illnesses.
This disorder is of the neurological type, and the brain is the central part affected by this. Someone with this disorder has trouble processing simple everyday sights and smells.
Apert syndrome is a autosomal dominant genetic disorder, meaning that only one copy of the mutated gene from either parent is necessary to inherit the condition. It is not sex-linked.
it means that you inherit this form of disorder either from your mother or father's sex chromosomes. For example- color blindness or Haemophillia.
SMA (spinal muscular atrophy) is typically inherited in an autosomal recessive pattern. This means that a child must inherit a copy of the faulty gene from both parents in order to develop the condition. In some rare cases, SMA can be inherited in an autosomal dominant pattern.
Sex-linked.
It has not been determined that "word blindness" is a genetic disorder. This colloquial term sometimes refers to dyslexia, a developmental communication disorder or alexia, an acquired communication disorder.
Blindness is typically considered a disability or impairment rather than a disease or disorder. It can be caused by a variety of factors such as injury, genetic conditions, or certain illnesses.
Marfan syndrome is an autosomal dominant disorder. An affected person has a 50% chance of passing it on to each offspring, regardless of gender.
color blindness is one
There is no cure for color blindness. It is a disorder that is passed from mother to son in fetal development and is genetic in nature.
Pleiotropy.
Its a pedigree. A pedigree shows the inheritance of a genetic disorder within a family and can help to determine the inheritance pattern and whether any particular individual has an allele for that disorder.
yes
Red-Green color blindness, or hemophilia.
There are so many genetic disorder caused by sex linked to name few; Auto Immune disorder, Hemophilia, Night Blindness etc.
The population of the United States of America are mostly affected by Binge Eating Disorder.