4.4 Article

An international classification of inherited metabolic disorders (ICIMD)

期刊

JOURNAL OF INHERITED METABOLIC DISEASE
卷 44, 期 1, 页码 164-177

出版社

WILEY
DOI: 10.1002/jimd.12348

关键词

classification; inherited metabolic disorders; ontology; ICIMD

资金

  1. Intramural NIH HHS [Z99 HG999999] Funding Source: Medline
  2. Medical Research Council [MC_UP_1002/1] Funding Source: Medline
  3. MRF [MRF_MRF-155-0002-RG-ZEVIA] Funding Source: Medline

向作者/读者索取更多资源

The International Classification of Inherited Metabolic Disorders (ICIMD) is a comprehensive classification system involving input from a large number of experts and endorsement from major metabolic societies globally. It aims to improve understanding of the interconnections between different conditions sharing similar characteristics, and guarantees continued relevance through regular curation and expert advice.
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.

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