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The rendering of human phenotype and rare diseases in ICD-11

ICD-11 (International Classification of Diseases, 11th Revision) is the next major revision of the ICD by the World Health Organization (WHO). ICD-11 differs dramatically from historical versions, as it is based on an underlying semantic network of terms and meaning, called the Foundation. To functi...

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Autor principal: Chute, Christopher G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959961/
https://www.ncbi.nlm.nih.gov/pubmed/29600497
http://dx.doi.org/10.1007/s10545-018-0172-5
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author Chute, Christopher G.
author_facet Chute, Christopher G.
author_sort Chute, Christopher G.
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description ICD-11 (International Classification of Diseases, 11th Revision) is the next major revision of the ICD by the World Health Organization (WHO). ICD-11 differs dramatically from historical versions, as it is based on an underlying semantic network of terms and meaning, called the Foundation. To function as a mutually exclusive and exhaustive statistical classification, ICD-11 creates derivative linearizations from the network that is a monohierarchy with residual categories such as Not Elsewhere Classified. ICD-11 also introduces the widespread post-coordination of terms, which allows for highly expressive representation of detailed patient descriptions. Phenotyping features are included in many subchapters or the signs and symptoms chapter. Composite phenotype descriptions of specific presentations or syndromes can be represented though post-coordination. Rare diseases are well represented in the Foundation, though not all appear in the relatively shallow linearization hierarchies.
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spelling pubmed-59599612018-05-24 The rendering of human phenotype and rare diseases in ICD-11 Chute, Christopher G. J Inherit Metab Dis Phenomics ICD-11 (International Classification of Diseases, 11th Revision) is the next major revision of the ICD by the World Health Organization (WHO). ICD-11 differs dramatically from historical versions, as it is based on an underlying semantic network of terms and meaning, called the Foundation. To function as a mutually exclusive and exhaustive statistical classification, ICD-11 creates derivative linearizations from the network that is a monohierarchy with residual categories such as Not Elsewhere Classified. ICD-11 also introduces the widespread post-coordination of terms, which allows for highly expressive representation of detailed patient descriptions. Phenotyping features are included in many subchapters or the signs and symptoms chapter. Composite phenotype descriptions of specific presentations or syndromes can be represented though post-coordination. Rare diseases are well represented in the Foundation, though not all appear in the relatively shallow linearization hierarchies. Springer Netherlands 2018-03-29 2018 /pmc/articles/PMC5959961/ /pubmed/29600497 http://dx.doi.org/10.1007/s10545-018-0172-5 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Phenomics
Chute, Christopher G.
The rendering of human phenotype and rare diseases in ICD-11
title The rendering of human phenotype and rare diseases in ICD-11
title_full The rendering of human phenotype and rare diseases in ICD-11
title_fullStr The rendering of human phenotype and rare diseases in ICD-11
title_full_unstemmed The rendering of human phenotype and rare diseases in ICD-11
title_short The rendering of human phenotype and rare diseases in ICD-11
title_sort rendering of human phenotype and rare diseases in icd-11
topic Phenomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959961/
https://www.ncbi.nlm.nih.gov/pubmed/29600497
http://dx.doi.org/10.1007/s10545-018-0172-5
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