Preferred Label : Patient Registry Study;
NCIt related terms : PATIENT REGISTRY;
Alternative definition : CDISC: Observational studies which include an organized system that uses observational
methods to collect uniform data (clinical and other) prospectively for a population
defined by a particular disorder/disease, condition (including susceptibility to a
disorder), or exposure (including products, health care services, and/or procedures)
and that serves a predetermined scientific, clinical, or policy purpose. Patient registries
may be single purpose or on-going data collection programs that address one or more
questions. (AHRQ);
Origin ID : C129000;
UMLS CUI : C0920631;
Semantic type(s)
- concept_is_in_subset
