Zwamborn-Hanssen A M, Bijlsma J B, Hennekam E F, Lindhout D, Beemer F A, Bakker E, Kleijer W J, de France H F, de Die-Smulders C E, Duran M, van Gennip A H, van Mens J T, Pearson P L, Mantel G, Verhage R E, Geraedts J P
Clinical Genetics Center Limburg, Maastricht, The Netherlands.
Am J Med Genet. 1997 Jun 27;70(4):444-7. doi: 10.1002/(sici)1096-8628(19970627)70:4<444::aid-ajmg20>3.0.co;2-g.
In medical genetics, several systems are used to classify and code genetic disorders for the purpose of automated registration. In the Netherlands, a genetic diagnosis code system has been developed that links a unique four-digit code to a principal description and all current synonyms. The main goal of this coding system is to enable nationwide uniformity of coding, without losing access to information stored in the past, identified by the ICD/BPA code (the International Classification of Diseases as adapted by the British Paediatric Association) and/or the MIM code (McKusick's classification in Mendelian Inheritance in Man). To this effect, the Dutch diagnosis code is cross-referenced with the 2 pre-existing classification systems. Developments in medical genetics make regular updates of all coding systems necessary. In the Netherlands, new diagnosis codes are assigned centrally to preserve uniformity and distributed periodically to all 8 clinical genetic centers. Diagnosis codes are assigned in numerical order of inclusion, enabling quick and easy updates. It is possible to include subclassifications of disorders according to pattern of inheritance, gene location, and gene mutations and to cover all disorders and disorder subtypes which are not clearly distinguished by the 2 pre-existing classification systems. The architecture of the coding system is suitable for international use. It offers a practical solution for clinical geneticists in need of a coding system suitable for clinical use. The use of the diagnosis code will also facilitate reliable comparison of data and nationwide genetic epidemiological studies.
在医学遗传学中,为了实现自动登记,使用了多种系统对遗传疾病进行分类和编码。在荷兰,已经开发了一种遗传诊断编码系统,该系统将一个唯一的四位数字编码与一个主要描述及所有当前同义词相链接。这个编码系统的主要目标是在全国范围内实现编码的一致性,同时又不会丢失通过ICD/BPA编码(英国儿科学会改编的国际疾病分类)和/或MIM编码(麦库西克的《人类孟德尔遗传》分类)所识别的过去存储的信息。为此,荷兰诊断编码与这两个先前存在的分类系统进行了交叉引用。医学遗传学的发展使得所有编码系统都需要定期更新。在荷兰,新的诊断编码由中央统一分配以保持一致性,并定期分发给所有8个临床遗传中心。诊断编码按纳入的数字顺序分配,便于快速轻松地更新。可以根据遗传模式、基因位置和基因突变对疾病进行细分,并涵盖这两个先前存在的分类系统未明确区分的所有疾病和疾病亚型。该编码系统的架构适合国际使用。它为需要适用于临床的编码系统的临床遗传学家提供了一个切实可行的解决方案。诊断编码的使用还将有助于可靠地比较数据和开展全国性的遗传流行病学研究。