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A cancer registry is a systematic collection of data about cancer and tumor diseases. The data are collected by Cancer Registrars. Cancer Registrars capture a complete summary of patient history, diagnosis, treatment, and status for every cancer patient in the United States, and other countries. [1]
Databases for oncogenomic research are biological databases dedicated to cancer data and oncogenomic research. They can be a primary source of cancer data, offer a certain level of analysis (processed data) or even offer online data mining.
SEER collects and publishes cancer incidence and survival data from population-based cancer registries covering approximately 34.6% of the population of the United States. SEER coverage includes 30.0% of African Americans , 44% of Hispanics, 49.3% of American Indians and Alaska Natives , 57.5% of Asians, and 68.5% of Hawaiian/Pacific Islanders ...
Frederick said data collected by a plethora of federal and state agencies play a key role in many of the organization's reports and publications, including the agency's "Cancer Statistics, 2025 ...
Cancer mortality rates are determined by the relationship of a population's health and lifestyle with their healthcare system. In the United States during 2013–2017, the age-adjusted mortality rate for all types of cancer was 189.5/100,000 for males, and 135.7/100,000 for females. [ 1 ]
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Testicular cancer: Fulton County, New York: 3 Dimethylformamide (DMF) 2-Ethoxyethanol 2-Ethoxyethyl acetate 2-Butoxyethanol [14] 1987–1999 Brain cancer, Leukemia, Lymphoma: Wilmington, Massachusetts: 20 Unknown N-Nitrosodimethylamine (NDMA) [15] [16] [17] 1993–2008 Childhood brain cancer, brain tumors, colon cancer, anal cancer, rectal ...
Three ZIP codes saw births fall more than 15% from 2019 through 2021. Skip to main content. 24/7 Help. For premium support please call: 800-290-4726 more ways to reach us. Sign in ...