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Genetics Home Reference (GHR) provides free access to consumer-friendly information on medical genetics to patients and their family members, health care professionals, and the public. The site offers summaries for a broad range of inherited conditions or disorders caused by gene alterations. Each condition summary includes the causes, available genetic testing, and links to summaries on related genes. Descriptions of genes include gene names and their synonyms, normal function, chromosome location, and an explanation of any disorder-causing mutations. Additionally, GHR provides a genetics glossary, help on understanding genetics, and links to many useful consumer, support, and research organizations. GHR is a service of the U.S. National Library of Medicine at the National Institutes of Health.

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Unique - Rare Chromosome Disorder Support Group for families affected by any rare chromosome disorder such as deletions, duplications, translocations, trisomy, monosomy, rings, mosaic, inversion, isodicentric, microdeletions, tetrasomy, monosomy, congenital, inherited

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Extensive knowledge base of medical information on symptoms, diagnosis, and misdiagnosis of more than 20,000 medical conditions. Research causes of your symptoms or research treatments for diseases.