We support precision medicine research for children with cancer, rare diseases and neurodevelopmental disorders.

Our outstanding researchers and clinicians are increasing capacity for rare disease research, innovation and equitable access to health system support for children with rare diseases and their families.

Grace is a fun-loving, kind and inquisitive eight-year-old girl who lives with ADCY5-related movement disorder syndrome, an ultra-rare genetic condition. Hear from Grace’s mother Emma and A/Prof Wendy Gold about how the Luminesce Alliance Functional Genomics Platform is supporting discovery to improve Grace’s function.