Medical Subject Headings

Last uploaded: April 29, 2019
Preferred Name

Motor Neuron Disease

Synonyms

Motor System Disease

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

Motor System Disease

Scleroses, Lateral

Lateral Scleroses, Primary

Sclerosis, Lateral

Neuron Diseases, Motor

Motor System Diseases

Motor Neuron Disease, Upper

Primary Lateral Scleroses

Neuron Disease, Motor

Secondary Motor Neuron Disease

Lateral Sclerosis

Primary Lateral Sclerosis

Lower Motor Neuron Disease

Familial Motor Neuron Disease

Anterior Horn Cell Disease

Upper Motor Neuron Disease

Motor Neuron Disease, Lower

Motor Neuron Diseases

Scleroses, Primary Lateral

Sclerosis, Primary Lateral

Motor Neuron Disease, Secondary

Lateral Sclerosis, Primary

Motor Neuron Disease, Familial

Lateral Scleroses

AN

GEN 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

C0521659

C0085084

C0543858

C0270763

C0154682

C0270764

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/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

Inverse of RO

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

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D000070627

http://purl.bioontology.org/ontology/MESH/D052879

http://purl.bioontology.org/ontology/MESH/D011051

http://purl.bioontology.org/ontology/MESH/D020361

http://purl.bioontology.org/ontology/MESH/D016750

http://purl.bioontology.org/ontology/MESH/D020271

http://purl.bioontology.org/ontology/MESH/D024801

http://purl.bioontology.org/ontology/MESH/D019578

http://purl.bioontology.org/ontology/MESH/D020511

http://purl.bioontology.org/ontology/MESH/D009135

http://purl.bioontology.org/ontology/MESH/D015673

http://purl.bioontology.org/ontology/MESH/D010300

http://purl.bioontology.org/ontology/MESH/D017096

http://purl.bioontology.org/ontology/MESH/D016262

http://purl.bioontology.org/ontology/MESH/D010523

http://purl.bioontology.org/ontology/MESH/D020961

http://purl.bioontology.org/ontology/MESH/D057177

Machine permutation

92

Mapped from

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

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

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

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

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

T372127

T372118

T372123

T049287

T372125

T372129

T372130

T372117

T372119

T002093

T372124

T372128

T372126

TH

UNK (19XX)

NLM (1992)

NLM (2000)

tui

T047

subClassOf

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

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

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