Preferred Name

颅缝早闭 / Craniosynostosis

Definitions

Craniosynostosis consists of premature fusion of one or more cranial sutures, resulting in an abnormal head shape. It can be divided in several subgroups; the major different types are primary vs secondary craniosynostosis and isolated vs syndromic craniosynostosis.

ID

http://purl.bmicc.cn/ontology/ICD11CN/LB70.0

definition

Craniosynostosis consists of premature fusion of one or more cranial sutures, resulting in an abnormal head shape. It can be divided in several subgroups; the major different types are primary vs secondary craniosynostosis and isolated vs syndromic craniosynostosis.

hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/458033798

inclusions

Imperfect fusion of skull

label

颅缝早闭 / Craniosynostosis

mappingRelation

http://purl.bmicc.cn/ontology/ICD10CN/Q75.0

notation

LB70.0

prefixIRI

ICD11CN:LB70.0

prefLabel

颅缝早闭 / Craniosynostosis

subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/LB70

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http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84655 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.obolibrary.org/obo/MONDO_0015469 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0015469 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/ICD10/Q75.0 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0010278 MedlinePlus Health Topics / MedlinePlus网站健康主题 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU002205 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/DOID_2340 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/HP_0001363 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q75.0 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 LOOM
http://www.orpha.net/ORDO/Orphanet_1531 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM