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The resources below were included to help connect those affected by HDFN to understanding communities and reliable information, and to assist in finding support programs and services.

Janssen has a relationship with the organizations and is not responsible for the support they provide.

Name About Phone Website
Allo Hope Foundation An organization that provides information about alloimmunization, promotes education, and offers access to resources and other relevant information
Global Genes An organization dedicated to eliminating the burdens and challenges of rare diseases for patients and families globally, united by a determination to support them and provide what they need to take action and thrive (949) 248-7273
National Organization for Rare Disorders (NORD) A patient advocacy organization committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient services (617) 249-7300

HDFN Information

Title Organization Description Link
Hemolytic Diseases of the Newborn National Library of Medicine Learn about HDFN and its history, epidemiology, and more.