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. 2021 Jan;44(1):164-177.
doi: 10.1002/jimd.12348.

An international classification of inherited metabolic disorders (ICIMD)

Collaborators, Affiliations

An international classification of inherited metabolic disorders (ICIMD)

Carlos R Ferreira et al. J Inherit Metab Dis. 2021 Jan.

Abstract

Several initiatives at establishing a classification of inherited metabolic disorders have been published previously, some focusing on pathomechanisms, others on clinical manifestations, while yet another attempted a simplified approach of a comprehensive nosology. Some of these classifications suffered from shortcomings, such as lack of a mechanism for continuous update in light of a rapidly evolving field, or lack of widespread input from the metabolic community at large. Our classification-the International Classification of Inherited Metabolic Disorders, or International Classification of Inborn Metabolic Disorders (ICIMD)-includes 1450 disorders, and differs from prior approaches in that it benefited from input by a large number of experts in the field, and was endorsed by major metabolic societies around the globe. Several criteria such as pathway involvement and pathomechanisms were considered. The main purpose of the hierarchical, group-based approach of the ICIMD is an improved understanding of the interconnections between many individual conditions that may share functional, clinical, and diagnostic features. The ICIMD aims to include any primary genetic condition in which alteration of a biochemical pathway is intrinsic to specific biochemical, clinical, and/or pathophysiological features. As new disorders are discovered, we will seek the opinion of experts in the advisory board prior to inclusion in the appropriate group of the ICIMD, thus guaranteeing the continuing relevance of this classification via regular curation and expert advice.

Keywords: ICIMD; classification; inherited metabolic disorders; ontology.

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Conflict of interest statement

Conflict of Interest:

Carlos Ferreira, Shamima Rahman and Johannes Zschocke declare that they have no conflict of interest.

Figures

Figure 1.
Figure 1.
Sunburst chart depicting the hierarchical nature of the International Classification of Inherited Metabolic Disorders. The size of each section of the chart is directly proportional to the number of disorders in that group. For an interactive version of the chart incorporating a zoom function, please refer to www.icimd.org.

References

    1. Brunk E, Sahoo S, Zielinski DC, et al. (2018) Recon3D enables a three-dimensional view of gene variation in human metabolism. Nat Biotechnol 36:272–281. 10.1038/nbt.4072 - DOI - PMC - PubMed
    1. Cortès-Saladelafont E, Tristán-Noguero A, Artuch R, et al. (2016) Diseases of the Synaptic Vesicle: A Potential New Group of Neurometabolic Disorders Affecting Neurotransmission. Semin Pediatr Neurol 23:306–320. 10.1016/j.spen.2016.11.005 - DOI - PubMed
    1. Dimauro S (2011) A history of mitochondrial diseases. J Inherit Metab Dis 34:261–276. 10.1007/s10545-010-9082-x - DOI - PubMed
    1. Fahy E, Subramaniam S, Brown HA, et al. (2005) A comprehensive classification system for lipids. J Lipid Res 46:839–861. 10.1194/jlr.E400004-JLR200 - DOI - PubMed
    1. Fahy E, Subramaniam S, Murphy RC, et al. (2009) Update of the LIPID MAPS comprehensive classification system for lipids. J Lipid Res 50 Suppl:S9–14. 10.1194/jlr.R800095-JLR200 - DOI - PMC - PubMed

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