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- Multi-Omics for Health and Disease (Multi-Omics)1
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Genetic Disorders
Prostate cancer is a disease where certain cells in the prostate become abnormal and multiply to form a tumor.
… whether genetic testing is appropriate for them. For more information about genetic counseling go to the Genetics Home … it to make sure that the testing will give you helpful information. … Symptoms: The symptoms of prostate cancer may … treatment is no longer working. Additional Resources of Information on Prostate Cancer Medline Plus: Prostate Cancer …
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.
… Association International National Digestive Diseases Information Clearing House Genetic and Rare Diseases Information Center Gene Tests Genetic Alliance National … Organization for Rare Disorders Finding Reliable Health Information Online … What is Wilson disease? … What are the …
Genetic Disorders
Duane syndrome is a rare, congenital eye movement disorder.
… Syndrome - Yahoo! Groups Genetics and Rare Diseases Information Center Finding Reliable Health Information Online … What is Duane syndrome? … What are the …
Genetic Disorders
Familial Mediterranean Fever is an inherited disease, characterized by recurrent attacks of fever, inflammation, painful, swollen joints, and ankle rash.
… Parent-to-Parent Network Genetics and Rare Diseases Information Center Finding Reliable Health Information Online … What is Familial Mediterranean Fever? … …
Genetic Disorders
Factor V Leiden thrombophilia is an inherited disorder of blood clotting.
… increasing the chance of developing abnormal blood clots. Information courtesy of: Genetics Home Reference … The … Factor V Leiden thrombophilia Finding Reliable Health Information Online … What is factor V Leiden thrombophilia? … …
Genetic Disorders
Holoprosencephaly is a disorder caused by the failure of the the embryonic forebrain to sufficiently divide into the double lobes of the cerebral hemispheres.
… About Holoprosencephaly NINDS Holoprosencephaly Information Page Carter Centers for Brain Research in …
Genetic Disorders
Neurofibromatosis is a genetic neurological disorder that can affect the brain, spinal cord, nerves and skin.
… the mutation analysis does not provide enough conclusive information. With at linkage analysis, blood tests from … Resources for Neurofibromatosis NINDS Neurofibromatosis Information Page Neurofibromatosis Network Medline Plus: …
Genetic Disorders
WAGR syndrome is a genetic condition caused by a deletion of genes located on chromosome 11, often causing eye problems and increased risk of cancer in babies.
… National Eye Institute (NEI) Genetics and Rare Diseases Information Center Finding Reliable Health Information Online … What is WAGR syndrome? … What are the …
Genetic Disorders
Tay-Sachs disease is a fatal genetic disorder that results in progressive destruction of the nervous system.
… Medline Plus: Tay-Sachs Disease NINDS: Tay-Sachs Disease Information Page Genetics Home Reference: Tay-Sachs disease …
Genetic Disorders
Spinal muscular atrophy is a group of inherited disorders that cause progressive muscle degeneration and weakness.
… Spinal muscular atrophy NINDS: Spinal Muscular Atrophy Information Page Genetics Home Reference: Spinal Muscular …