Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Huntington Disease

Synonyms

Akinetic-Rigid Variant of Huntington Disease

Definitions

A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)

ID

http://purl.bioontology.org/ontology/MESH/D006816

altLabel

Akinetic-Rigid Variant of Huntington Disease

Huntington Disease, Late Onset

Late Onset Huntington Disease

Progressive Chorea, Hereditary, Chronic (Huntington)

Chorea, Huntington

Juvenile-Onset Huntington Disease

Huntington's Chorea

Huntington Disease, Late-Onset

Progressive Chorea, Chronic Hereditary (Huntington)

Huntington Disease, Akinetic-Rigid Variant

Huntington Disease, Akinetic Rigid Variant

Juvenile Huntington Disease

Juvenile Onset Huntington Disease

Huntington Disease, Juvenile

Chorea, Huntington's

Huntington Disease, Juvenile-Onset

Chorea, Chronic Progressive Hereditary (Huntington)

Huntington Disease, Juvenile Onset

Late-Onset Huntington Disease

Huntington Chorea

Akinetic Rigid Variant of Huntington Disease

Huntington Chronic Progressive Hereditary Chorea

Chronic Progressive Hereditary Chorea (Huntington)

Huntington's Disease

AQL

BL CF CI CL 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

C0751207

C0393574

C0751208

C0020179

DC

1

definition

A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)

DX

20000101

HN

2000(1963)

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/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/D054546

http://purl.bioontology.org/ontology/MESH/D015418

http://purl.bioontology.org/ontology/MESH/D028227

http://purl.bioontology.org/ontology/MESH/D013494

http://purl.bioontology.org/ontology/MESH/D020232

http://purl.bioontology.org/ontology/MESH/D007562

http://purl.bioontology.org/ontology/MESH/D020144

http://purl.bioontology.org/ontology/MESH/D020279

http://purl.bioontology.org/ontology/MESH/D016098

http://purl.bioontology.org/ontology/MESH/D038261

http://purl.bioontology.org/ontology/MESH/D017825

http://purl.bioontology.org/ontology/MESH/D055956

http://purl.bioontology.org/ontology/MESH/D038901

http://purl.bioontology.org/ontology/MESH/D009224

http://purl.bioontology.org/ontology/MESH/D014897

http://purl.bioontology.org/ontology/MESH/D009459

http://purl.bioontology.org/ontology/MESH/D017253

http://purl.bioontology.org/ontology/MESH/D015417

http://purl.bioontology.org/ontology/MESH/D014402

http://purl.bioontology.org/ontology/MESH/D006527

http://purl.bioontology.org/ontology/MESH/D057174

http://purl.bioontology.org/ontology/MESH/D001308

http://purl.bioontology.org/ontology/MESH/D006211

http://purl.bioontology.org/ontology/MESH/D005879

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

http://purl.bioontology.org/ontology/MESH/D003057

http://purl.bioontology.org/ontology/MESH/D020150

http://purl.bioontology.org/ontology/MESH/D015140

http://purl.bioontology.org/ontology/MESH/D020734

http://purl.bioontology.org/ontology/MESH/D020192

http://purl.bioontology.org/ontology/MESH/D009223

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

http://purl.bioontology.org/ontology/MESH/D055534

http://purl.bioontology.org/ontology/MESH/D018888

http://purl.bioontology.org/ontology/MESH/D009477

http://purl.bioontology.org/ontology/MESH/D060825

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

http://purl.bioontology.org/ontology/MESH/D000544

http://purl.bioontology.org/ontology/MESH/D020194

http://purl.bioontology.org/ontology/MESH/D009472

http://purl.bioontology.org/ontology/MESH/D008538

http://purl.bioontology.org/ontology/MESH/D004422

http://purl.bioontology.org/ontology/MESH/D015526

Machine permutation

2000; see HUNTINGTON'S DISEASE 1993-1999; for HUNTINGTON DISEASE see HUNTINGTON'S DISEASE 1993-1999, see HUNTINGTON CHOREA 1977-1992, see CHOREA, HEREDITARY 1963-1976

Mapped from

http://purl.bioontology.org/ontology/MESH/C565747

http://purl.bioontology.org/ontology/MESH/C566398

http://purl.bioontology.org/ontology/MESH/C536694

MDA

19990101

MMR

20150630

MN

C10.228.140.079.545

F03.615.400.390

C10.574.500.497

C16.320.400.430

F03.615.250.400

C10.228.662.262.249.750

C10.228.140.380.278

notation

D006816

prefLabel

Huntington Disease

TERMUI

T020579

T364197

T364189

T364194

T368476

T364196

T364187

T364236

T020576

T364208

T364186

T364235

T020578

T364188

T364201

T364195

T020577

TH

BIOETHICS (1974)

NLM (1993)

NLM (1978)

NLM (2000)

ORD (2010)

OMIM (2013)

NLM (19XX)

GHR (2014)

tui

T047

subClassOf

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

http://purl.bioontology.org/ontology/MESH/D001480

http://purl.bioontology.org/ontology/MESH/D003704

http://purl.bioontology.org/ontology/MESH/D003072

http://purl.bioontology.org/ontology/MESH/D002819

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