|Trisomy 18 Foundation
||Founded by Victoria J. Miller, M.A. in 2003, she and her husband Don are the parents of a baby son, Isaac lost to Trisomy 18 at 11 days old .
||9TIPS is an international support group for families dealing with Trisomy 9 covering all variations.
|| is an advocacy organization composed primarily of the parents of individuals with a chromosome 18 abnormality.
|Hope for Trisomy
||created in honor and memory of all living and nonliving children with Trisomy 13 and 18 and Related Conditions.
||Support Group for people with a 4th chromosome
||is specifically designed and supported for the benefit of families of children with Distal Trisomy 10q (also called Partial Trisomy 10q).
|Chromosome 22 Central
||is a parent run support organization. Offers basic information on the main chromosome 22 disorders
||aims to provide much needed, non-judgemental support to families, friends and relatives during this difficult time.
|| is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them.