Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
Preferred Name

Cerebral Palsy

Synonyms

Cerebral Palsy, Monoplegic, Infantile

Definitions

A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)

ID

http://purl.bioontology.org/ontology/MESH/D002547

altLabel

Cerebral Palsy, Monoplegic, Infantile

Monoplegic Infantile Cerebral Palsy

Cerebral Palsy, Dyskinetic

Cerebral Palsy, Rolandic Type

Cerebral Palsy, Hypotonic

Cerebral Palsy, Dystonic Rigid

Hypotonic Cerebral Palsy

Infantile Cerebral Palsy, Quadriplegic

Dystonic-Rigid Cerebral Palsy

Little Disease

Diplegic Infantile Cerebral Palsy

Infantile Cerebral Palsy, Monoplegic

Cerebral Palsy, Dystonic-Rigid

Atonic Cerebral Palsy

Cerebral Palsy, Congenital

Spastic Diplegia

Spastic Diplegias

Diplegia, Spastic

Cerebral Palsies, Athetoid

Monoplegic Cerebral Palsies

Monoplegic Cerebral Palsy

Cerebral Palsy, Atonic

Cerebral Palsy, Diplegic, Infantile

CP (Cerebral Palsy)

Infantile Cerebral Palsy, Diplegic

Spastic Cerebral Palsies

Mixed Cerebral Palsies

Cerebral Palsy, Quadriplegic, Infantile

Little's Disease

Dystonic-Rigid Cerebral Palsies

Cerebral Palsies, Dystonic-Rigid

Hypotonic Cerebral Palsies

Quadriplegic Infantile Cerebral Palsy

Spastic Cerebral Palsy

Mixed Cerebral Palsy

Diplegias, Spastic

Cerebral Palsies, Dyskinetic

Cerebral Palsy, Monoplegic

Cerebral Palsy, Spastic

Dyskinetic Cerebral Palsy

Cerebral Palsy, Athetoid

Cerebral Palsies, Monoplegic

Athetoid Cerebral Palsy

Rolandic Type Cerebral Palsy

Cerebral Palsy, Mixed

Congenital Cerebral Palsy

AN

do not index under MUSCLE SPASTICITY unless especially discussed & then only NIM

AQL

BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C0270742

C0553767

C0007789

C0154697

C0338596

C0394007

C0394003

C0023882

C0270807

C0751024

C0154695

C0154698

C0751025

DC

1

definition

A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)

DX

19660101

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Mapped from

http://purl.bioontology.org/ontology/MESH/C537945

http://purl.bioontology.org/ontology/MESH/C565587

http://purl.bioontology.org/ontology/MESH/C567858

http://purl.bioontology.org/ontology/MESH/C536143

http://purl.bioontology.org/ontology/MESH/C567853

http://purl.bioontology.org/ontology/MESH/C565610

http://purl.bioontology.org/ontology/MESH/C538101

http://purl.bioontology.org/ontology/MESH/C537761

http://purl.bioontology.org/ontology/MESH/C567867

http://purl.bioontology.org/ontology/MESH/C562856

MDA

19990101

MMR

20030725

MN

C10.228.140.140.254

notation

D002547

prefLabel

Cerebral Palsy

TERMUI

T367028

T367026

T367046

T367027

T367044

T367009

T367030

T367031

T007419

T367010

T367035

T367045

T367036

T367034

T007423

T367043

T367008

T367049

T367047

T367011

T007420

T367048

T367032

T367029

T367033

T007421

T367050

TH

UNK (19XX)

NLM (2000)

NLM (1966)

NLM (1995)

tui

T019

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D001925

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http://purl.bioontology.org/ontology/MEDLINEPLUS/C0007789 MedlinePlus Health Topics / MedlinePlus网站健康主题 CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0007789 MedlinePlus Health Topics / MedlinePlus网站健康主题 LOOM
http://purl.obolibrary.org/obo/DOID_1969 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_1969 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/ICD10/G80.0 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://www.ebi.ac.uk/efo/EFO_1000632 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/ICD10/G80.1 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.obolibrary.org/obo/HP_0100021 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU006625 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bmicc.cn/ontology/ICD10CN/G80.3 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/LNC/LP74604-7 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.bioontology.org/ontology/LNC/LP74604-7 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34460 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.bioontology.org/ontology/ICD10CM/G80.1 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/ICD10CM/G80.1 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/ICD10CM/G80 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/ICD10CM/G80 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/LNC/LA27858-2 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.bioontology.org/ontology/LNC/LA27858-2 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU044330 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU044330 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/MONDO_0006497 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.bioontology.org/ontology/LNC/MTHU020800 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.bioontology.org/ontology/LNC/MTHU020800 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bioontology.org/ontology/ICD10CM/G80.9 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bmicc.cn/ontology/ICD10CN/G80.0 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.bmicc.cn/ontology/ICD10CN/G80.1 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.bmicc.cn/ontology/ICD11CN/L1-8D2 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/ICD10CM/G80.3 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/ICD10/G80.3 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU033921 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU027939 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI