Using Online Mendelian Inheritance in Man in low- and middle-income countries

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Abstract

Online Mendelian Inheritance in Man (OMIMĀ®), an online catalog of human genes and genetic disorders, has been used in the low- and middle-income countries largely as a tool for improving clinical care, teaching genetics and genomics, and for clinical and research analysis of next-generation sequencing. By facilitating free access to curated, updated, and comprehensive information in genetics and genomics, OMIM has led to better clinical care and research advancement in countries where clinicians and researchers in private or public hospitals and universities cannot afford to pay for other resources including journal subscriptions.

Description

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Citation

de Macena Sobreira NL, Repetto GM, Temtamy SA, Alvarez Perez AB. Using Online Mendelian Inheritance in Man in low- and middle-income countries. Am J Med Genet A. 2021 Nov;185(11):3284-3286. doi: 10.1002/ajmg.a.62467.

Keywords

Diagnosis, Education, Low-income countries, Middle-income countries, OMIM, Rare diseases

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