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Permission to conduct the study was also obtained from the participating health facilities. Signed informed consent was obtained from the study subjects before data collection. We did not include personally identifiable information in the dataset. Blood and stool samples were collected for the health facilities\u2019 own use; thus, we did not hold any biological specimen. Data collectors advised anemic cases on dietary management of anemia and the importance of further medical care. Refer to this study\u2019s registration status through its ClinicalTrials.gov identifier (NCT number: NCT03251664) available on .","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethical standards"}}]}}