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- Developmental Genotype-Tissue Expression (dGTEx)1
- Multi-Omics for Health and Disease (Multi-Omics)1
- Ethical, Legal and Social Implications (ELSI) Research Program2
- Genomics-Enabled Learning Health Systems (gLHS)2
- Genetic Architecture of Complex Traits1
- Genome Technology Program1
- Impact of Genomic Variation on Function (IGVF) Consortium3
- Molecular Phenotypes of Null Alleles in Cells (MorPhiC)1
- Clinical Genome (ClinGen) Resource1
- Genomic Innovator Awards1
- Polygenic RIsk MEthods in Diverse populations (PRIMED) Consortium1
- NHGRI Genomic Data Science Analysis, Visualization and Informatics Lab-space (AnVIL)2
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium2
Genetic Disorders
Prostate cancer is a disease where certain cells in the prostate become abnormal and multiply to form a tumor.
… For more information about genetic counseling go to the Genetics Home Reference . There are companies that will soon … Plus: Prostate Cancer NCI: Prostate Cancer Information Genetics Home Reference: Prostate Cancer Zerocancer.org GARD: …
Genetic Disorders
Sickle cell disease is a group of inherited red blood cells disorders.
… Sickle Cell Disease NIH Fact Sheet: Sickle Cell Disease Genetics Home Reference: Sickle Cell Disease GARD: Sickle …
Genetic Disorders
Colon cancer is a malignant tumor of the large intestine that affects both men and women.
… Cancer National Cancer Institute Colon Cancer Alliance Genetics and Rare Diseases Information Center Familial adenomatous polyposis - Genetics Home Reference Lynch Syndrome - Genetics Home Reference Do You Know Tony? Family History of …
Genetic Disorders
Hemophilia is a bleeding disorder that slows down the blood clotting process.
… GeneReviews: Hemophilia A GeneReviews: Hemophilia B Genetics Home Reference: Hemophilia Medline Plus: Hemophilia …
Genetic Disorders
Skin cancer is the most common type of cancer in the United States.
… Skin Cancer NCI: Skin Cancer The Skin Cancer Foundation Genetics Home Reference: Melanoma … How prevalent is skin …
Genetic Disorders
Familial hypercholesterolemia is an inherited condition causing increased low density lipoprotein cholesterol at birth and heart attacks at an early age.
… Treating Genetic Diseases: Familial Hypercholesterolemia Genetics and Rare Diseases Information Center Finding …
Genetic Disorders
Thalassemia is a group of inherited diseases of the blood that affect a person's ability to produce hemoglobin, resulting in anemia.
… Thalassemia NHLBI: Thalassemias Medline Plus: Thalassemia Genetics Home Reference: Beta thalassemia Thalassemia.com …
Genetic Disorders
Spinal muscular atrophy is a group of inherited disorders that cause progressive muscle degeneration and weakness.
… atrophy NINDS: Spinal Muscular Atrophy Information Page Genetics Home Reference: Spinal Muscular Atrophy Muscular …
Genetic Disorders
Charcot-Marie-Tooth disease is an inherited neurological disease characterized by a slowly progressive degeneration of the muscles and loss of sensation.
… Charcot-Marie-Tooth Disease Charcot Marie Tooth Disease - Genetics Home Reference National Organization for Rare … Page National Center for Biotechnology Information Genetics and Rare Diseases Information Center Finding …
Genetic Disorders
Klinefelter syndrome is a condition that occurs in men as a result of an extra X chromosome. The most common symptom is infertility.
… adulthood. Additional Resources for Klinefelter Syndrome Genetics Home Reference: Klinefelter syndrome Medline Plus: …