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• 8th International Symposium on Mucopolysaccharide and Related Diseases - The 8th International Symposium on MPS and Related Diseases will be held in Mainz, Germany. Traditionally, this symposium unites scientists, patients and their parents to share and discuss recent scientific results.
• Alliance of Genetic Support Groups - Nnational coalition of consumers, professionals, and genetic support groups to voice the common concerns of children, adults, and families living with, and at risk for, genetic conditions.
• Blue Cone Monochromacy - A discussion board for those affected by BCM. Read the contents, search and post from this location.
• Chromosome 18 Issues - A support and awareness discussion board for people affected by this disorder.
• Chromosome 22 Central - Support group for families who have children with any chromosome 22 disorder, including trisomies, cat eye syndrome, translocations, deletions 22q11, 22q13, VCFS, Digeorge syndrome, rings and unique malformations.
• Chromosome Deletion Outreach, Inc. (CDO) - Non-profit voluntary support group for families affected by rare chromosome disorders.
• Chromosome Help-Station - Information on rare chromosomal disorders. Support and advice for families.
• Cornelia de Lange Syndrome (CdLS) Foundation Outreach - Family support organization which exists to ensure the early and accurate diagnosis of CdLS, promote research into the causes and manifestations of the syndrome, and help people with a diagnosis of CdLS, and others with similar characteristics, make informed decisions throughout their lifetime.
• Friedreichs's Ataxia Network - Support group providing some answers and up to date information on local support and worldwide research being conducted. Based in Brisbane.
• Ideas - A support group for families and professionals interested in the chromosomal condition known as isodicentric 15 (formerly inverted duplication 15).
• Lafora body disease research talk - This is a discussion group about lafora body disease.
• Nobellybutton - For adult survivors of gastroschisis, omphaloceles, or other abdominal wall defects.
• Online Genetic Syndrome Support Groups - Sites are listed alphabetically by disease/condition.
• Parents of Polydactyly and Webbed Children - A support board for those parents of children born with extra toes/fingers as well as webbing. A place to learn new information and make friends with others
• Peter's Anomaly Support Group - An online support group for people dealing with Peter's Anomaly.
• S.O.F.T. - A United Kingdom support organisation for parents of infants with Trisomy 13 and 18 and other related disorders.
• S.O.F.T. - Support Organization in the United States for Trisomy 18, 13, and other related disorders. Provides literature, conferences, newsletter, chapter information, and international contacts.
• The Rainbow - A forum for people who have chromosome abnormalites to show support, give advice and comfort.
• Unique Rare Chromosome Disorder Support Group - Support and information for families of children with rare disorders.
• Yahoo Groups Floating Harbor - An active support site for the parents and families of children with Floating Harbor Syndrome.
• Search our Wiki for Conditions Diseases Genetic - Find more information about this subject by clicking here