cerebellar ataxia

Preferred Label : cerebellar ataxia;

MeSH definition : Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90);

MeSH synonym : incoordinations, cerebellar; cerebellar incoordinations; cerebellar ataxias; ataxias, cerebellar; cerebellar incoordination; incoordination, cerebellar; ataxia, cerebellar;

MeSH hyponym : hypermetria; cerebellar hemiataxia; adiadochokinesis; cerebellar dysmetria; Cerebellar Hemiataxias; Hemiataxia, Cerebellar; Hemiataxias, Cerebellar; Cerebellar Dysmetrias; Dysmetria, Cerebellar; Dysmetrias, Cerebellar; Dysmetria; Dysmetrias; Hypermetrias; Adiadochokineses;

MeSH annotation : DENTATE CEREBELLAR ATAXIA see MYOCLONIC CEREBELLAR DYSSYNERGIA is also available; ATAXIAS, HEREDITARY see SPINOCEREBELLAR DEGENERATION is also available;

Wikipedia link : https://en.wikipedia.org/wiki/Cerebellar ataxia;

Details

Origin ID

D002524;

UMLS CUI

C0007758;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- ADIADOKOKINESIS [WHO-ART Included Term]
- Adiadochokinesia (finding) [SNOMED CT concept]
- Adiadokokinesis [MedDRA LLT]
- DYSMETRIA [WHO-ART Included Term]
- Dysmetria [ICD-11 More detail]
- Dysmetria [MedDRA Preferred Term]
- Dysmetria [MedDRA LLT]
- Dysmetria (finding) [SNOMED CT concept]
- Hypermetria [MedDRA LLT]
- Hypermetria (finding) [SNOMED CT concept]
- Other and unspecified lack of coordination [ICD-10 Sub-category (who)]
- Other cerebellar ataxia [ICD-9 code]
- Past pointing (finding) [SNOMED CT concept]
- abnormal involuntary movements [ICPC-2 Rubric]
- adiadochokinesia [SNOMED Notion]
- dysmetria, nos [SNOMED Notion]
- hypermetria [SNOMED Notion]
Currated CISMeF NLP mapping
- ATAXIA CEREBELLAR [WHO-ART Preferred Term]
- Ataxia cerebellar [MedDRA LLT]
- Cerebellar ataxia [PASCAL descriptor]
- Cerebellar ataxia [MedDRA Preferred Term]
- Cerebellar ataxia (disorder) [SNOMED CT concept]
- cerebellar ataxia [DO Concept]
- cerebellar ataxia [Disease (Nov.)]
- cerebellar ataxia, nos [SNOMED Notion]
DO Cross reference
- cerebellar ataxia [DO Concept]
False automatic mappings
- Ataxia [HPO term]
- Dysmetria [NCIt concept]
HPO term
- Ataxia [HPO term]
- Dysmetria [HPO term]
Indexing information
- CACNA1A protein, human [MeSH Supplementary Concept]
- Cacna1a protein, rat [MeSH Supplementary Concept]
Record concept(s)
- adiadochokinesis [MeSH concept]
- cerebellar ataxia [MeSH concept]
- cerebellar dysmetria [MeSH concept]
- cerebellar hemiataxia [MeSH concept]
- hypermetria [MeSH concept]
Related MeSH Supplementary Concept(s)
- 3-Methylglutaconic aciduria, type V [MeSH Supplementary Concept]
- Brachydactyly-Nystagmus-Cerebellar ataxia [MeSH Supplementary Concept]
- CANVAS syndrome [MeSH Supplementary Concept]
- CAPOS syndrome [MeSH Supplementary Concept]
- Mainzer-Saldino disease [MeSH Supplementary Concept]
- Marinesco-Sjogren-like syndrome (MSLS) [MeSH Supplementary Concept]
- aniridia cerebellar ataxia mental deficiency [MeSH Supplementary Concept]
- ataxia, spastic, 1, autosomal dominant [MeSH Supplementary Concept]
- ataxia, spastic, 2, autosomal recessive [MeSH Supplementary Concept]
- ataxia, spastic, 3, autosomal recessive [MeSH Supplementary Concept]
- autosomal recessive cerebellar ataxia type 1 [MeSH Supplementary Concept]
- branchial myoclonus with spastic paraparesis and cerebellar ataxia [MeSH Supplementary Concept]
- cerebellar ataxia and hypergonadotropic hypogonadism [MeSH Supplementary Concept]
- cerebellar ataxia and hypogonadotropic hypogonadism [MeSH Supplementary Concept]
- cerebellar ataxia and neurosensory deafness [MeSH Supplementary Concept]
- cerebellar ataxia ectodermal dysplasia [MeSH Supplementary Concept]
- cerebellar ataxia, benign, with thermoanalgesia [MeSH Supplementary Concept]
- cerebellar ataxia, cayman type [MeSH Supplementary Concept]
- cerebellar ataxia, deafness, and narcolepsy [MeSH Supplementary Concept]
- cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 [MeSH Supplementary Concept]
- cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 [MeSH Supplementary Concept]
- cerebellar hypoplasia with endosteal sclerosis [MeSH Supplementary Concept]
- cerebelloparenchymal disorder II [MeSH Supplementary Concept]
- dementia, familial danish [MeSH Supplementary Concept]
- dysequilibrium syndrome [MeSH Supplementary Concept]
- early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MeSH Supplementary Concept]
- episodic ataxia, type 5 [MeSH Supplementary Concept]
- episodic ataxia, type 6 [MeSH Supplementary Concept]
- furukawa takagi nakao syndrome [MeSH Supplementary Concept]
- harding ataxia [MeSH Supplementary Concept]
- hemiplegic migraine, familial type 1 [MeSH Supplementary Concept]
- herrmann syndrome [MeSH Supplementary Concept]
- laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy [MeSH Supplementary Concept]
- myelocerebellar disorder [MeSH Supplementary Concept]
- myoclonus, cerebellar ataxia, and deafness [MeSH Supplementary Concept]
- neuhauser eichner opitz syndrome [MeSH Supplementary Concept]
- renal tubulopathy, diabetes mellitus, and cerebellar ataxia due to duplication of mitochondrial DNA [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Dysmetria [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ATAXIA CEREBELLAR [WHO-ART Preferred Term]
- Ataxia [HPO term]
- Ataxia cerebellar [MedDRA LLT]
- Cerebellar ataxia [MedDRA Preferred Term]
- Cerebellar ataxia [PASCAL descriptor]
- Cerebellar ataxia (disorder) [SNOMED CT concept]
- cerebellar ataxia [DO Concept]
- cerebellar ataxia [Disease (Nov.)]
- cerebellar ataxia, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- dysmetria [Disease (Nov.)]

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