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Genetic Disorders
Wilson disease is a rare genetic condition that causes a person's body to store too much of the mineral copper, leading to organ damage that may cause death.
… water checked for copper content. … Yes. Wilson disease is inherited in what doctors call an autosomal (not on the X … Disease Association International National Digestive Diseases Information Clearing House Genetic and Rare Diseases … … How is Wilson disease treated? … Is Wilson disease inherited? … About Wilson Disease … Wilson disease is a rare …
Fact Sheets
Genetics refers to the study of genes and their roles in inheritance. Genomics refers to the study of all of a person's genes (the genome).
… of cells and functions of the body. Examples of genetic or inherited disorders include cystic fibrosis (See: Learning … Genomics includes the scientific study of complex diseases such as heart disease, asthma, diabetes, and cancer … such as sickle cell anemia and cystic fibrosis are inherited in families, what screening and testing options are …
For Patients and Families
Neglected diseases are conditions that inflict severe health burdens on the world's poorest people.
… Neglected diseases are conditions that inflict severe health burdens on … or by others instrumental in drug access. … Neglected diseases are conditions that inflict severe health burdens on … poorest people. Many of these conditions are infectious diseases that are most prevalent in tropical climates, …
For Patients and Families
​Genetic research is creating new ways for people to take action and prevent disease and new ways to treat disease through personalized medicine.​ ​
… medicine. … We have known for a long time that common diseases like heart disease, asthma, cancer, and diabetes can run in families. Rare diseases like hemophilia, cystic fibrosis, and sickle cell … you have an increased chance of getting some common diseases. Your health care provider can then give you …
Genetic Disorders
Parkinson's disease is a neurological condition that typically causes tremor and/or stiffness in movement
… came from a small town in Southern Italy in which PD was inherited from parent to child (dominant inheritance). We found the gene that caused their inherited Parkinson's Disease and it coded for a protein … to identify genetic variations that contribute to common diseases including Parkinson's disease. … In most cases …
Genetic Disorders
Dercum disease is a rare condition that is characterized by multiple, painful fatty tumors that occur chiefly in post-menopausal, obese women of middle age.
… in families, and in some of these cases it seems to be inherited as an autosomal dominant trait (this means that one out of a person's two copies of the gene, inherited from one parent, is altered). However, most …
Genetic Disorders
Alpha-1 antitrypsin deficiency is an inherited condition that causes low levels of, or no, alpha-1 antitrypsin in the blood.
… Alpha-1 antitrypsin deficiency is an inherited condition that causes low levels of, or no, alpha-1 … the blood. … Alpha-1 antitrypsin deficiency (AATD) is an inherited condition that causes low levels of, or no, alpha-1 … benefit most. … Alpha-1 antitrypsin deficiency (AATD) is inherited in families in an autosomal codominant pattern. …
News Release
As researchers uncover millions of DNA differences in genes, doctors struggle to know which of these inherited differences, called variants, really matter.
… genes. But doctors have struggled to know which of these inherited differences - variants - really matter. … For the … to apply these standards in the context of particular diseases. ClinGen projects center on developing processes and … in genes, doctors have struggled to know which of these inherited differences (variants) really matter. ​ … Genomic …
Educational Resources
Sickle cell disease is a hereditary disease seen most often among people of African ancestry.
… of African ancestry. … Autosome, Birth Defect, Gene, Inherited, Mutation, Protein, Recessive … Sickle cell disease … genes that encode the hemoglobin protein, the disease is inherited as an autosomal recessive trait. The mutation …
Genetic Disorders
Crohn's disease is a chronic inflammatory disorder of the bowel, usually diagnosed in people between the ages of 20 - 30.
… skin problems; kidney stones, gallstones or other diseases of the liver and biliary system. Both men and women … Treating Children and Adolescents National Digestive Diseases Information Clearinghouse Inflammatory Bowel Disease … is the treatment for Crohn's disease? … Is Crohn's disease inherited? … About Crohn's Disease … Crohn's disease is a …