When a question is about a specific case, Ai4RD searches named sources: medical research, rare-disease databases, and guides written for patients. These searches stay inside those sites:
- PubMed — the U.S. National Library of Medicine’s index of peer-reviewed medical research.
- Orphanet — the reference database of rare diseases and orphan drugs.
- NORD — the National Organization for Rare Disorders.
- GARD — the NIH Genetic and Rare Diseases Information Center.
There is also a general web search, for questions those databases don’t cover. It isn’t limited to a list of sites. Ai4RD is told to use only trusted clinical and scientific sources there too, but that is an instruction, not a hard limit — so read those results as you would any web result. The Sources list always shows where a claim came from.
Every full answer ends with that list, so a clinician can check the reasoning against the research. If a search finds nothing, Ai4RD says so instead of inventing a reference.