This website provides information and communication about biliary atresia to the general public and a secure area for healthcare professionals.

Biliary Atresia Network is an online support group for families who are dealing with pediatric liver disease, biliary atresia pre- or post-transplant.

This foundation is devoted to providing support for research and education into the causes, diagnoses, prevention and treatment of all liver disease.

ChiLDRN Supports the discovery of new diagnostics, etiologic and treatment options for children with liver disease, and those who undergo liver transplantation.

C.L.A.S.S. is a nonprofit, all-volunteer organization, dedicated to serving the emotional, educational and financial needs of families confronting childhood liver disease and transplantation.

COTA exists to assist patients who require a life-saving transplant by providing fundraising assistance and family support.

The National Organization for Rare Disorders (NORD) provides advocacy, education and other services to improve the lives of all people affected by rare diseases.

PALF aims at identifying, characterizing, and developing management strategies for infants, children, and adolescents who present with acute liver failure.