The XLH Network is a patient support organization for individuals living with X-Linked Hypophosphatemia (XLH), focusing on awareness, education, and community support.

The XLID98 Foundation supports individuals affected by the ultra-rare neurodevelopmental condition XLID98, also known as NEXMIF, KIAA2022, and KIDLIA, and aims to promote awareness and research for treatment.

The XLP Research Trust supports families affected by X-Linked Lymphoproliferative disease and funds research into XLP1 and XIAP.

The YWHAG Research Foundation raises awareness and educates the public about the YWHAG genetic mutation, supporting families affected by this rare neurological disorder.

ZERO TO THREE is dedicated to promoting the healthy development of infants and toddlers through research-based resources, training, and advocacy for policies that support early childhood education and well-being.

The ZMYND11 Treatment Foundation focuses on supporting families affected by the rare ZMYND11 gene disorder and aims to find treatments to improve the function of the ZMYND11 protein and alleviate symptoms.