The map of the registry, by category.
Nine sections covering the resources medical scientists actually reach for. Each card is a curated entry into a domain — open it to see every resource we hold, with editor's notes and cross-references.
Literature & clinical references
Indexes, archives and decision-support — the published record of medicine.
Disease knowledge bases
Compendia, ontologies and terminologies that name disease unambiguously.
Rare disease databases
Nomenclatures, registries and patient-led portals for the 7,000+ conditions in the long tail.
Genetic & genomic
Variants, populations, gene–disease curation and deep phenotyping.
Cancer databases
Somatic mutations, multi-omic cohorts, actionability and surveillance.
Infectious disease & surveillance
Pathogen genomes, surveillance portals and real-time outbreak intelligence.
Specialty disease databases
Single-domain registries and cohorts where specialist data accumulates.
Drug & chemical–disease
Targets, indications, toxicology — chemicals and the diseases they touch.
Phenotype, pathway & integrative
Pathways, phenotypes and the connective tissue that links the rest.