Preferred Name

脑裂畸形 / Schizencephaly

Definitions

Schizencephaly is a rare congenital cerebral malformation characterized by the presence of linear clefts in one or both hemispheres of the brain, extending from the lateral ventricles to the pial surface of the cortex, and that lead to a variety of neurological symptoms such as epilepsy, motor deficits, and psychomotor retardation.

ID

http://purl.bmicc.cn/ontology/ICD11CN/LA05.61

definition

Schizencephaly is a rare congenital cerebral malformation characterized by the presence of linear clefts in one or both hemispheres of the brain, extending from the lateral ventricles to the pial surface of the cortex, and that lead to a variety of neurological symptoms such as epilepsy, motor deficits, and psychomotor retardation.

hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/1693546163

label

脑裂畸形 / Schizencephaly

mappingRelation

http://purl.bmicc.cn/ontology/ICD10CN/Q00-Q07

notation

LA05.61

prefixIRI

ICD11CN:LA05.61

prefLabel

脑裂畸形 / Schizencephaly

subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/LA05.6

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http://purl.bioontology.org/ontology/MESH/D065707 Medical Subject Headings LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99056 National Cancer Institute Thesaurus LOOM
http://purl.bioontology.org/ontology/OMIM/269160 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU029060 Online Mendelian Inheritance in Man LOOM