Database: NORDCAN (European Union): Difference between revisions
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{{forresearchers}} | {{forresearchers}} | ||
'''Type of Database:''' [[databaseType::registry]] | |||
'''Primary purpose:''' To provide a freely accessible database of comparable cancer statistics for the Nordic countries. | '''Primary purpose:''' To provide a freely accessible database of comparable cancer statistics for the Nordic countries. | ||
Revision as of 19:25, 27 May 2024
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Type of Database: registry
Primary purpose: To provide a freely accessible database of comparable cancer statistics for the Nordic countries.
Sponsor, manager or home institution: The Association of the Nordic Cancer Registries (ANCR).
Type of information: Number of new cancer cases (incidence); Cancer mortality; Number of individuals living with a cancer diagnosis (prevalence); cancer survival; age; Country; year; sex. Click here to learn more.
Source of Information: The sources vary from each national cancer registry and cause of death registry.
Data level: national level.
Number of Records: unknown.
Date range: 1943 onwards.
Cancer Areas of Interest: C00-D48: All neoplasms. Click here to learn more.
Data access: publicly available. Click here to access. You can visualize the data using factsheets, click here to access or interactive visualization tools click here to access.
Contact information: Click here to access.
