Hemochromatosis
Epilepsy is not a genetic disorder. It is a physical condition and can have a whole range of causes. Epilepsy has a wide range of forms and has been known of for thousands of years. So it is not really known who discovered it.
There are dozens of diseases caused by a genetic defect. They are known as genetic diseases. Sickle Cell anemia, Hemophilia, Tay-Sachs, Huntingtons Disease- and many others are genetic diseases.
it is a type of neural tube defect or known as a birth defect
Yes, bipolar disorder is known to have a genetic component. Research shows that individuals with a family history of bipolar disorder are at a higher risk of developing the condition themselves. However, genetics is just one factor that contributes to the development of bipolar disorder, and environmental factors also play a role.
A genetic disorder in which the essential digestive enzyme phenylalanine hydroxylase is missing is known as Phenylketonuria (PKU). This leads to a buildup of phenylalanine in the body, which can be toxic to the brain if not managed properly through a restricted diet low in phenylalanine.
Gene Therapy
The most common known genetic cause of autism spectrum disorder is mutations in the genes responsible for regulating brain development and function. These mutations can disrupt communication between brain cells and affect how the brain processes information, leading to the symptoms of autism.
The disease which causes what is popularly known as a werewolf is an inherited genetic disorder called hypertrichosis. To become a werewolf, then, you would have to be born to a couple who carry the correct genetic material. In other words, you cannot become a werewolf without having the disorder.
No, Hunter Syndrome (also known as Mucopolysaccharidosis type II) is a rare genetic disorder that affects metabolism. It is caused by the lack of an enzyme in the body. On the other hand, Huntington's chorea (also known as Huntington's disease) is a different genetic disorder that affects the brain, leading to movement, cognitive, and psychiatric symptoms. While both are genetic disorders, they affect different systems in the body.
Yes, Brittle Bone Disease, also known as Osteogenesis Imperfecta, is a genetic disorder. It is caused by a gene mutation that affects the body's ability to produce collagen, resulting in brittle and fragile bones that are prone to fractures. The severity of the condition can vary depending on the specific gene mutation involved.
Because Huntington's is a genetic disorder and it is known what sequence in what region causes the disorder.
RA is an Auto immune disorder and its cause is not known. however there seem to often be genetic factors involved.