Skip to main content
. Author manuscript; available in PMC: 2024 Jul 8.
Published in final edited form as: Nat Genet. 2024 Feb;56(2):189–193. doi: 10.1038/s41588-023-01642-1

Fig. 1 |. A model for advancing the diagnosis of rare diseases in Indigenous people.

Fig. 1 |

The figure summarizes key themes (such as incorporating Indigenous world views) as well as core elements (such as co-design, strengths-based approaches, and the sovereignty and governance of Indigenous data), and resulting outputs (such as trust, and culturally safe and responsive solutions) for both Indigenous and non-Indigenous people (two-way learning).