Genetics & Molecular Medicine terms
Inherited variation, genomics, molecular markers, and targeted molecular care. Browse definitions and meanings below.
Terms in this topic
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A rare disorder caused by loss of part of the long arm (Q arm) of human chromosome 5.
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A rare disorder caused by loss of part of the long arm (Q arm) of human chromosome 5.
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A substance being studied in the treatment of breast cancers caused by mutations (changes) in the BRCA1 and BRCA2 genes.
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A genetic condition in which tumors form on the nerves of the inner ear and cause loss of hearing and balance.
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A chemical compound that is used to make one of the building blocks of DNA and RNA.
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A substance present in all living cells that provides energy for many metabolic processes and is involved in making RNA.
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An inherited disorder marked by rapid aging that begins in early adolescence.
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A substance being studied in the treatment of breast cancers caused by mutations (changes) in the BRCA1 and BRCA2 genes.
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A group of genetic conditions marked by little or none of the pigment melanin in the skin, hair, and/or eyes.
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An inherited immune disorder that occurs in young boys.
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A procedure in which a person receives stem cells (cells from which all blood cells develop) from a genetically similar, but not identical, donor.
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A procedure in which a person receives blood-forming stem cells (cells from which all blood cells develop) from a genetically similar, but not identical, donor.
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A substance that is being studied as a gene therapy agent in the treatment of cancer.
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A type of anticancer drug that blocks cell growth by interfering with DNA, the genetic material in cells.
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A type of anticancer drug that blocks cell growth by interfering with DNA, the genetic material in cells.
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A type of gene that makes a protein called a tumor suppressor protein that helps control cell growth.
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Small pieces of DNA or RNA that can bind to specific molecules of RNA.
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Small pieces of DNA or RNA that can bind to specific molecules of RNA.
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A type of anticancer drug that blocks cell growth by interfering with DNA, the genetic material in cells.
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A rare, inherited, progressive, degenerative disease of childhood that causes loss of muscle control, a weakened immune system, and an increased risk of cancer.