in the spleen because that is the most active part of the body besides the heart
Genetic mutations passed from parent to child cause hereditary disease.
Viral, bacterial, or hereditary? In viral diseases, the virus can just be dormant in the parents, but in the child it isn't.
Depends on the disease- dominant gene or recessive gene- and the genotypes of the parents.
No. While it is a hereditary disease it is not at all a bleeding disorder, nor is it only passed by the mother. It is a degenerative, neuropsychiatric disease that can be passed by either the mother or father. If the parent has it, the child's chance of inheritance is of the faulty gene is 50%.
no albinism is a hereditary.
A hereditary disease is carried because one of the parents has broken DNA (meaning, the DNA is not normal and the loss of one part of the DNA caused the hereditary disease), and that broken DNA is copied to every cell in the body, and when the two sex cells join together, there is broken DNA in one of the sex cells, thereby officially passing the hereditary disease to the next child.
Yes. It is possible to carry the gene(s) for a hereditary disease without the disease ever being expressed. The chance of a child inheriting the disease, rather than just being a carrier like its parents, depends on the disease and on whether one or both parents has the gene. A genetic counselor or clinical geneticist would be able to give the chances for a child having a specific disease.
Orthopnea is not hereditary. It is a symptom of a disease.
Gayness
The disease was hereditary in their family.
No.
A disease is more probable to affect a child than an adult because the adult body has lived more and its body maybe already knows the disease. but the child's body has lived for a little period of time so the child's body doesn't know the disease so it ends up getting the disease.