Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Muscular Atrophy, Spinal
Synonyms

Neuronopathies, Hereditary Motor
Definitions

A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)
ID

http://purl.bioontology.org/ontology/MESH/D009134
altLabel

Neuronopathies, Hereditary Motor

Progressive Muscular Atrophies

Adult Spinal Muscular Atrophy

Neuronopathy, Bulbospinal

Muscular Atrophy, Myelopathic

Bulbospinal Neuronopathy

Atrophy, Spinal Muscular

Spinal Muscular Atrophy

Atrophy, Progressive Muscular

Amyotrophy, Spinal

Bulbospinal Neuronopathies

Motor Neuronopathies, Hereditary

Myelopathic Muscular Atrophy, Progressive

Neuronopathies, Bulbospinal

Progressive Muscular Atrophy

Scapuloperoneal Form of Spinal Muscular Atrophy

Myelopathic Muscular Atrophy

Proximal Myelopathic Muscular Atrophy, Progressive

Adult Onset Spinal Muscular Atrophy

Amyotrophy, Neurogenic Scapuloperoneal, New England Type

Spinal Muscular Atrophy, Oculopharyngeal

Spinal Muscular Atrophy, Scapuloperoneal Form

Adult-Onset Spinal Muscular Atrophy

Oculopharyngeal Spinal Muscular Atrophy

Neuronopathy, Hereditary Motor

Spinal Amyotrophy

Muscular Atrophy, Adult Spinal

Progressive Myelopathic Muscular Atrophy

Atrophy, Myelopathic Muscular

Spinal Muscular Atrophy, Distal

Progressive Proximal Myelopathic Muscular Atrophy

Spinal Muscular Atrophy, Scapuloperoneal

Atrophies, Progressive Muscular

Distal Spinal Muscular Atrophy

Hereditary Motor Neuronopathies

Muscular Atrophies, Progressive

Hereditary Motor Neuronopathy

Amyotrophies, Spinal

Muscular Atrophy, Progressive

Spinal Amyotrophies

Scapuloperoneal Spinal Muscular Atrophy

Motor Neuronopathy, Hereditary
AN

MUSCULAR ATROPHY, SPINAL, INFANTILE see SPINAL MUSCULAR ATROPHIES OF CHILDHOOD is also available
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

C0393541

C0917981

C0393546

C0751335

C3661519

C0751334

C0393547

C0270765

C0026847
DC

1
definition

A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)
DX

19880101
HN

1988
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 SIB

http://purl.bioontology.org/ontology/MESH/D020758

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

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

http://purl.bioontology.org/ontology/MESH/D013119

http://purl.bioontology.org/ontology/MESH/D010244

http://purl.bioontology.org/ontology/MESH/D063205

http://purl.bioontology.org/ontology/MESH/D009187

http://purl.bioontology.org/ontology/MESH/D020802

http://purl.bioontology.org/ontology/MESH/D013595

http://purl.bioontology.org/ontology/MESH/D000690

http://purl.bioontology.org/ontology/MESH/D013132

http://purl.bioontology.org/ontology/MESH/D013120

http://purl.bioontology.org/ontology/MESH/D013606

http://purl.bioontology.org/ontology/MESH/D013117
Machine permutation

1988
Mapped from

http://purl.bioontology.org/ontology/MESH/C536880

http://purl.bioontology.org/ontology/MESH/C566673

http://purl.bioontology.org/ontology/MESH/C566670

http://purl.bioontology.org/ontology/MESH/C563443

http://purl.bioontology.org/ontology/MESH/C567084

http://purl.bioontology.org/ontology/MESH/C563562

http://purl.bioontology.org/ontology/MESH/C535715

http://purl.bioontology.org/ontology/MESH/C563948

http://purl.bioontology.org/ontology/MESH/C564362

http://purl.bioontology.org/ontology/MESH/C563561

http://purl.bioontology.org/ontology/MESH/C580044

http://purl.bioontology.org/ontology/MESH/C566672

http://purl.bioontology.org/ontology/MESH/C566674

http://purl.bioontology.org/ontology/MESH/C564506

http://purl.bioontology.org/ontology/MESH/C536881

http://purl.bioontology.org/ontology/MESH/C563981

http://purl.bioontology.org/ontology/MESH/C537968

http://purl.bioontology.org/ontology/MESH/C564807

http://purl.bioontology.org/ontology/MESH/C564626

http://purl.bioontology.org/ontology/MESH/C566695

http://purl.bioontology.org/ontology/MESH/C566675

http://purl.bioontology.org/ontology/MESH/C538417
MDA

19870310
MMR

20150623
MN

C10.668.467.500

C10.574.562.500

C10.228.854.468
notation

D009134
prefLabel

Muscular Atrophy, Spinal
TERMUI

T369609

T369581

T812434

T027301

T369611

T752490

T369610

T369616

T369612

T369614

T369608

T027303

T812433

T369615

T812432

T369585

T369613

T842507

T027302

T842508

T752489

T369584

T027300
TH

UNK (19XX)

NLM (2000)

NLM (2010)

ORD (2010)

NLM (1988)

OMIM (2013)

GHR (2014)
tui

T047
subClassOf

http://purl.bioontology.org/ontology/MESH/D013118

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