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The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research

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dc.contributor.author Yalcouye, A.
dc.contributor.author Hotchkiss, J.
dc.contributor.author Manyisa, N.
dc.contributor.author Adadey, S.M.
dc.contributor.author Oluwole, O.G.
dc.contributor.author Wonkam, E.
dc.contributor.author Mnika, K.
dc.contributor.author Yalcouye, A.
dc.contributor.author Nembaware, V.
dc.contributor.author Haendel, M.
dc.contributor.author Vasilevsky, N.
dc.contributor.author Mulder, N.J.
dc.contributor.author Jupp, S.
dc.contributor.author Wonkam, A.
dc.contributor.author Mazandu, G.K.
dc.date.accessioned 2019-12-16T09:09:33Z
dc.date.available 2019-12-16T09:09:33Z
dc.date.issued 2019-11-21
dc.identifier.other doi:10.3390/genes10120960
dc.identifier.uri http://ugspace.ug.edu.gh/handle/123456789/34195
dc.description Research Article en_US
dc.description.abstract Hearing impairment (HI) is a common sensory disorder that is defined as the partial or complete inability to detect sound in one or both ears. This diverse pathology is associated with a myriad of phenotypic expressions and can be non-syndromic or syndromic. HI can be caused by various genetic, environmental, and/or unknown factors. Some ontologies capture some HI forms, phenotypes, and syndromes, but there is no comprehensive knowledge portal which includes aspects specific to the HI disease state. This hampers inter-study comparability, integration, and interoperability within and across disciplines. This work describes the HI Ontology (HIO) that was developed based on the Sickle Cell Disease Ontology (SCDO) model. This is a collaboratively developed resource built around the ‘Hearing Impairment’ concept by a group of experts in di erent aspects of HI and ontologies. HIO is the first comprehensive, standardized, hierarchical, and logical representation of existing HI knowledge. HIO allows researchers and clinicians alike to readily access standardized HI-related knowledge in a single location and promotes collaborations and HI information sharing, including epidemiological, socio-environmental, biomedical, genetic, and phenotypic information. Furthermore, this ontology illustrates the adaptability of the SCDO framework for use in developing a disease-specific ontology en_US
dc.description.sponsorship The development and implementation of the HIO is funded by the National Institutes of Health (NIH) Common Fund grants U01-HG-009716 and 1U01HG007459-01 to AW and the African Academy of Science/Wellcome Trust Ref H3A/18/001 and 1U54HG009790-01 to AW. Some developers and ontologists are supported by the National Heart, Lung, and Blood Institute of the National Institutes of Health under Award Number U24HL135600 to AW. en_US
dc.language.iso en en_US
dc.publisher Genes en_US
dc.relation.ispartofseries 10;960
dc.subject hearing impairment en_US
dc.subject hearing loss en_US
dc.subject ontology en_US
dc.subject data harmonization en_US
dc.subject meta-analysis en_US
dc.title The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research en_US
dc.type Article en_US


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