Beckwith-Wiedemann Syndrome 2
Down Syndrome 26
| | Genetic Disorders - Conditions and Diseases, Health 707
 Alliance of Genetic Support GroupsAlliance of Genetic Support Groups
 National 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.
|
Chromosome 22 CentralChromosome 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 malformations.
|
Chromosome Deletion Outreach, Inc. (CDO)Chromosome Deletion Outreach, Inc. (CDO)
 Non-profit voluntary support group for families affected by rare chromosome disorders.
|
Chromosome Help-StationChromosome Help-Station
 Information on rare chromosomal disorders. Support and advice for families.
|
Cornelia de Lange Syndrome (CdLS) Foundation OutreachCornelia 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.
|
Distal Trisomy 10q FamiliesDistal Trisomy 10q Families
 Support for families of children with Distal Trisomy 10q. Family stories, contacts, other information.
|
Forum for Patients with Myotonic Dystrophy 2Forum for Patients with Myotonic Dystrophy 2
 A forum for sharing information, increasing public awareness, and building advocacy for further research for patients diagnosed with Myotonic Dystrophy Type 2.
|
GendersInX.orgGendersInX.org
 Support and encouragement for people with congenital gender variations.
|
IdeasIdeas
 A support group for families and professionals interested in the chromosomal condition known as isodicentric 15 (formerly inverted duplication 15).
|
Lafora body disease research talkLafora body disease research talk
 This is a discussion group about lafora body disease.
|
Online Genetic Syndrome Support GroupsOnline Genetic Syndrome Support Groups
 Sites are listed alphabetically by disease/condition.
|
Oto-Palatal-Digital Syndrome Family Resource NetworkOto-Palatal-Digital Syndrome Family Resource Network
 Resources, articles, support and general information on the rare disorder, Oto-Palatal-Digital Syndrome.
|
Parents of Polydactyly and Webbed ChildrenParents 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 GroupPeter's Anomaly Support Group
 An online support group for people dealing with Peter's Anomaly.
|
The RainbowThe Rainbow
 A forum for people who have chromosome abnormalites to show support, give advice and comfort.
|
S.O.F.T.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.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.
|
Thomas Scott DavidsonThomas Scott Davidson
 This is a memorial website for Thomas Scott Davidson who died from Anencephaly.
|
Trisomy 18 AngelTrisomy 18 Angel
 This site was made in memory of our daughter Abigail Renee, to help other families who have been given a diagnosis of Trisomy 18.
|
Trisomy 18 MomsTrisomy 18 Moms
 Lists Trisomy 18, Edwards syndrome memorial site, help making a website, and share a story.
|
Trisomy 18 Support Online CommunityTrisomy 18 Support Online Community
 Participate in this support group for those pregnant with, parenting, or grieving the loss of child with Trisomy 18. Includes resources for all stages of the journey.
|
Unique Rare Chromosome Disorder Support GroupUnique Rare Chromosome Disorder Support Group
 Support and information for families of children with rare disorders.
|
Who is EPI ?Who is EPI ?
 The mission of the European Porphyria Initiative (EPI) is to present an up to date approach to the understanding of porphyria.
|
X-Linked Alpha Thalassemia M/R SyndromeX-Linked Alpha Thalassemia M/R Syndrome
 Features a Yahoo! group for family support for individuals caring for others affected by "Alpha Thalassemia Mental Retardation Syndrome (ATR-X).
|
Yahoo Groups Floating HarborYahoo Groups Floating Harbor
 An active support site for the parents and families of children with Floating Harbor Syndrome.
|
Yahoo Support Group for CMT-HMSN-HNPPYahoo Support Group for CMT-HMSN-HNPP
 A very active support group that prides itself on helping its members through the good - bad days and posting the latest CMT/HMSN/HNPP research information available on the web.
|
|
