Preferred Name

脊柱裂 / Spina bifida

Definitions

Spina bifida is the most common of a group of birth defects called neural tube defects. Spina bifida affects the backbone and, sometimes, the spinal cord. Aperta spina bifida defines the dorsal malclosure of vertebrae, associated with various degrees of spine defects. A pocket of skin may form, containing meninges (meningocele) or spinal cord and meninges (myelomeningocele). Different subtypes are distinguished according to the location of the defect. Consequences are paraplegia (paralysed lower limbs), hydrocephaly, Chiari malformation (result of the attached spine during life in utero), urinary and anorectal incontinence. The intensity of signs varies greatly with the level and extent of the lesion.

ID

http://purl.bmicc.cn/ontology/ICD11CN/LA02

definition

Spina bifida is the most common of a group of birth defects called neural tube defects. Spina bifida affects the backbone and, sometimes, the spinal cord. Aperta spina bifida defines the dorsal malclosure of vertebrae, associated with various degrees of spine defects. A pocket of skin may form, containing meninges (meningocele) or spinal cord and meninges (myelomeningocele). Different subtypes are distinguished according to the location of the defect. Consequences are paraplegia (paralysed lower limbs), hydrocephaly, Chiari malformation (result of the attached spine during life in utero), urinary and anorectal incontinence. The intensity of signs varies greatly with the level and extent of the lesion.

exclusions

Arnold-Chiari malformation type I (LA07.4)

Occult spinal dysraphism (LB73.0)

Arnold-Chiari malformation type II (LA03)

free_Translation

http://purl.bmicc.cn/ontology/ICD10CN/Q05

has_exact_match

http://purl.bmicc.cn/ontology/ICD10CN/Q05

hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/2036217905

inclusions

Syringomyelocele

Myelomeningocele

Rachischisis

Myeloschisis

Spinal dysraphism

label

脊柱裂 / Spina bifida

notation

LA02

prefixIRI

ICD11CN:LA02

prefLabel

脊柱裂 / Spina bifida

subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/L2-LA0

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http://purl.obolibrary.org/obo/DOID_0080016 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_0080016 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0008449 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU007928 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C101214 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://www.ebi.ac.uk/efo/EFO_0003105 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q05 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 LOOM
http://purl.bioontology.org/ontology/ICD10/Q05 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.obolibrary.org/obo/HP_0002414 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/LNC/LA19643-8 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM