Search Results
Genetic Disorders
Alpha-1 antitrypsin deficiency is an inherited condition that causes low levels of, or no, alpha-1 antitrypsin in the blood.
… of, or no, alpha-1 antitrypsin in the blood. … Genetic Disorders …
Genetic Disorders
Huntington's disease is an inherited neurological illness causing involuntary movements, severe emotional disturbance and cognitive decline.
… emotional disturbance and cognitive decline. … Genetic Disorders …
Genetic Disorders
Velocardiofacial syndrome is the most common syndrome associated with a cleft palate.
… common syndrome associated with a cleft palate. … Genetic Disorders …
Genetic Disorders
Turner syndrome is a chromosomal condition that alters development in females.
… condition that alters development in females. … Genetic Disorders …
Genetic Disorders
Hereditary hemochromatosis is a genetic disease that alters the body's ability to regulate iron absorption.
… the body's ability to regulate iron absorption. … Genetic Disorders …
Genetic Disorders
Familial Mediterranean Fever is an inherited disease, characterized by recurrent attacks of fever, inflammation, painful, swollen joints, and ankle rash.
… painful, swollen joints, and ankle rash. … Genetic Disorders …
Genetic Disorders
Cystic fibrosis is a genetic disease that causes the body to produce thick, sticky mucus that clogs the lungs, leads to infection, and blocks the pancreas.
… leads to infection, and blocks the pancreas. … Genetic Disorders …
Genetic Disorders
Cri du chat syndrome is a rare genetic condition that is caused by the deletion of genetic material on the the p arm of chromosome 5.
… material on the the p arm of chromosome 5. … Genetic Disorders …
Genetic Disorders
Breast cancer is the second most common cancer in women after skin cancer.
… most common cancer in women after skin cancer. … Genetic Disorders …
Genetic Disorders
Colon cancer is a malignant tumor of the large intestine that affects both men and women.
… large intestine that affects both men and women. … Genetic Disorders …