This data set contains counts of AIDS (Acquired Immune Deficiency Syndrome) cases reported to CDC by state and local health departments from 1981+. Case counts can be retrieved by demographics, case-definition, date of diagnosis, date of report, HIV exposure group (risk factors), and mortality.
Medicare Australia provides health-related statistics that play a valuable role in assisting health professionals, researchers and journalists as well as the general public.
The Australian Institute of Health and Welfare (AIHW) is a major national agency set up by the Australian Government under the Australian Institute of Health and Welfare Act to provide reliable, regular and relevant information and statistics on Australia's health and welfare.
The aim of the project is to provide contemporary estimates of the incidence of, mortality and prevalence from major types of cancer, at national level, for 184 countries of the world.
One of NHMRC’s primary roles is to fund high quality health and medical research and ensure that the Australian community receives the health and economic benefits from that investment. An important part of this responsibility includes enabling researchers and members of the community to access the outputs of research.
NHMRC encourages data sharing and providing access to data and other research outputs (metadata, analysis code, study protocols, study materials and other collected data) arising from NHMRC supported research.
Examines national health systems from 1960 forward for OECD member countries in a general, demographic, economic, and social context.
The World Health Organization is an agency of the United Nations and is an international coordinating agency for public health.
Data and Statistics: Major WHO databases include the Global Health Observatory (national statistics for health indicators), WHO Global Infobase Online (chronic diseases and risk factors), and the Global Health Atlas. Data is also accessible by topical categories.
The Yale University Open Data Access (YODA) Project’s mission is to advocate for the responsible sharing of clinical research data, open science, and research transparency. The Project is committed to supporting research focused on improving the health of patients and informing science and public health.