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Preferred Name

联合免疫缺陷 / Combined immunodeficiencies
ID

http://purl.bmicc.cn/ontology/ICD11CN/4A01.1
Coded_Elsewhere

Laron syndrome with immunodeficiency (5A61.0)
exclusions

autosomal recessive agammaglobulinaemia (Swiss type) (4A01.00)
free_Translation

http://purl.bmicc.cn/ontology/ICD10CN/D81
has_exact_match

http://purl.bmicc.cn/ontology/ICD10CN/D81
hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/1616506198
label

联合免疫缺陷 / Combined immunodeficiencies
notation

4A01.1
prefixIRI

ICD11CN:A01.1
prefLabel

联合免疫缺陷 / Combined immunodeficiencies
subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/4A01
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http://purl.bioontology.org/ontology/ICD10CM/D81 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://purl.bioontology.org/ontology/ICD10/D81 International Classification of Diseases, Version 10 LOOM