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Preferred Name

原发性肌肉功能障碍 / Primary disorders of muscles
ID

http://purl.bmicc.cn/ontology/ICD11CN/L2-8C7
Coded_Elsewhere

Idiopathic rhabdomyolysis (FB32.20)

Idiopathic inflammatory myopathy (4A41)
exclusions

Arthrogryposis multiplex congenita (LD26.41)

Metabolic disorders (BlockL1‑5C5)
hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/833816211
label

原发性肌肉功能障碍 / Primary disorders of muscles
mappingRelation

http://purl.bmicc.cn/ontology/ICD10CN/G71
notation

L2-8C7
prefixIRI

ICD11CN:L2-8C7
prefLabel

原发性肌肉功能障碍 / Primary disorders of muscles
subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/L1-8C6
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http://purl.bioontology.org/ontology/ICD10/G71 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.bioontology.org/ontology/ICD10CM/G71 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 LOOM