Medical Subject Headings

Last uploaded: January 31, 2024
Preferred Name

Motor Neuron Disease

Synonyms

Familial Motor Neuron Disease

Sclerosis, Lateral

Definitions

Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)

ID

http://purl.bioontology.org/ontology/MESH/D016472

altLabel

Familial Motor Neuron Disease

Sclerosis, Primary Lateral

Motor Neuron Diseases

Motor System Diseases

Primary Lateral Sclerosis

Motor Neuron Disease, Lower

Scleroses, Lateral

Lateral Scleroses

Primary Lateral Scleroses

Lateral Sclerosis, Primary

Neuron Disease, Motor

Secondary Motor Neuron Disease

Neuron Diseases, Motor

Upper Motor Neuron Disease

Motor Neuron Disease, Familial

Motor System Disease

Motor Neuron Disease, Secondary

Lateral Scleroses, Primary

Scleroses, Primary Lateral

Lower Motor Neuron Disease

Motor Neuron Disease, Upper

Anterior Horn Cell Disease

Lateral Sclerosis

Sclerosis, Lateral

AN

general or unspecified; prefer specifics

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

C0154681

C0270763

C0085084

C0154682

C0270764

C0521659

C0543858

DC

1

definition

Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)

DX

19920101

HN

92

Inverse of AQ

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Inverse of RO

http://purl.bioontology.org/ontology/MESH/D009046

Machine permutation

92

Mapped from

http://purl.bioontology.org/ontology/MESH/C563517

http://purl.bioontology.org/ontology/MESH/C566900

http://purl.bioontology.org/ontology/MESH/C567502

http://purl.bioontology.org/ontology/MESH/C536416

http://purl.bioontology.org/ontology/MESH/C563954

MDA

19910621

MMR

20100625

MN

C10.574.562

C10.668.467

notation

D016472

prefLabel

Motor Neuron Disease

TERMUI

T372117

T002093

T372128

T372119

T372125

T372127

T372130

T372129

T049287

T372123

T372118

T372126

T372124

TH

NLM (2000)

NLM (1992)

UNK (19XX)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D009468

http://purl.bioontology.org/ontology/MESH/D019636

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http://purl.bioontology.org/ontology/MDRGER/10002696 MDRGER CUI
http://purl.bioontology.org/ontology/MDRGER/10071328 MDRGER CUI
http://purl.bioontology.org/ontology/MSHFRE/D016472 MSHFRE CUI
http://purl.bioontology.org/ontology/MSHFRE/D016472 MSHFRE CUI
http://purl.bioontology.org/ontology/OMIM/MTHU075081 OMIM CUI
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http://purl.bioontology.org/ontology/MDRFRE/10045639 MDRFRE CUI
http://purl.bioontology.org/ontology/MDRGER/10045639 MDRGER CUI
http://purl.bioontology.org/ontology/MEDDRA/10045639 MEDDRA CUI
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http://purl.bioontology.org/ontology/MEDDRA/10002694 MEDDRA CUI
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http://purl.bioontology.org/ontology/SNMI/DA-23001 SNMI CUI
http://purl.bioontology.org/ontology/MDRGER/10071338 MDRGER CUI
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http://purl.bioontology.org/ontology/MSHFRE/D016472 MSHFRE CUI
http://purl.bioontology.org/ontology/ICD10CM/G12.2 ICD10CM CUI
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http://purl.bioontology.org/ontology/ICD10CM/G12.23 ICD10CM CUI
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http://purl.bioontology.org/ontology/CSP/2057-3603 CRISP CUI
http://purl.bioontology.org/ontology/RCD/F1524 RCD CUI
http://purl.bioontology.org/ontology/SNMI/DA-23012 SNMI CUI
http://purl.bioontology.org/ontology/ICD9CM/335.24 ICD9CM CUI
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http://purl.bioontology.org/ontology/SCTSPA/84590007 SCTSPA CUI
http://purl.bioontology.org/ontology/OMIM/MTHU002948 OMIM CUI
http://purl.bioontology.org/ontology/SNOMEDCT/84590007 SNOMEDCT CUI
http://purl.bioontology.org/ontology/SNMI/DA-23040 SNMI CUI
http://purl.bioontology.org/ontology/MSHFRE/D016472 MSHFRE CUI
http://purl.bioontology.org/ontology/SNOMEDCT/95647008 SNOMEDCT CUI
http://purl.bioontology.org/ontology/SNMI/DA-23003 SNMI CUI
http://purl.bioontology.org/ontology/SCTSPA/95647008 SCTSPA CUI
http://www.ebi.ac.uk/efo/EFO_0003782 EFO LOOM
http://purl.obolibrary.org/obo/DOID_231 DOID LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/37340000 SNOMEDCT LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C197818 NCIT LOOM
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http://purl.bioontology.org/ontology/ICD10CM/G12.2 ICD10CM LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0085084 OCHV LOOM
http://purl.obolibrary.org/obo/ND_0000119 NDDO LOOM
http://purl.obolibrary.org/obo/ND_0000119 NIO LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038384 PMAPP-PMO LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12565 NIFDYS LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12565 NIFSTD LOOM
http://bioontology.org/projects/ontologies/birnlex#birnlex_12565 BIRNLEX LOOM
http://www.limics.org/hrdo/rdfns#pat_id_13520 HRDO LOOM
http://doe-generated-ontology.com/OntoAD#C0085084 ONTOAD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D016472 RH-MESH LOOM
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http://www.orpha.net/ORDO/Orphanet_98503 ORDO LOOM
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http://purl.obolibrary.org/obo/DOID_231 DTO LOOM
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http://purl.obolibrary.org/obo/DOID_231 NIFSTD LOOM
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http://purl.jp/bio/4/id/200906065489984726 IOBC LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU036400 OMIM LOOM
http://www.gamuts.net/entity#motor_neuron_disease GAMUTS LOOM
http://purl.obolibrary.org/obo/OMIT_0016965 OMIT LOOM
http://purl.bioontology.org/ontology/ICPC2P/N99010 ICPC2P LOOM