ataxia - CISMeF

Preferred Label : ataxia;

MeSH definition : Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions.;

MeSH synonym : coordination impairment; ataxias; impairment, coordination; dyssynergia; coordination impairments; impairments, coordination; ataxy;

MeSH hyponym : incoordination; ataxia, appendicular; ataxia, truncal; ataxia, motor; tremor, rubral; ataxia, sensory; dyscoordination; Ataxias, Motor; Motor Ataxia; Motor Ataxias; Rubral Tremor; Rubral Tremors; Tremors, Rubral; Ataxias, Truncal; Truncal Ataxia; Truncal Ataxias; Lack of Coordination; Coordination Lack; Incoordinations; Appendicular Ataxia; Appendicular Ataxias; Ataxias, Appendicular; Ataxia, Limb; Ataxias, Limb; Limb Ataxia; Limb Ataxias; Ataxias, Sensory; Sensory Ataxia; Sensory Ataxias;

MeSH annotation : note specifics; coord other ataxias with organ/diseases term; enzootic SWAYBACK; familial: consider also SPINOCEREBELLAR DEGENERATIONS;

Wikipedia link : https://en.wikipedia.org/wiki/Ataxia;

Details

Origin ID

D001259;

UMLS CUI

C0004134;

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)
- Ataxia, CTCAE 5.0 [NCIt concept]
- Ataxia, unspecified [ICD-10 Sub-category (who)]
- Ataxic [MedDRA LLT]
- Dyssynergia [HPO term]
- Holmes tremor [MedDRA Preferred Term]
- INCOORDINATION [WHO-ART Included Term]
- Incoordination [HPO term]
- Incoordination [MedDRA LLT]
- Kinetic ataxia [MedDRA LLT]
- Lack of coordination [MedDRA LLT]
- Limb ataxia [LOINC component]
- Limb ataxia [HPO term]
- Motor ataxia [MedDRA LLT]
- Motor ataxia (finding) [SNOMED CT concept]
- Muscular incoordination (finding) [SNOMED CT concept]
- No incoordination (situation) [SNOMED CT concept]
- Other lack of coordination [ICD-10 category (who)]
- Rubral tremor [HPO term]
- Rubral tremor (finding) [SNOMED CT concept]
- Sensory ataxia [HPO term]
- Sensory ataxia [MedDRA LLT]
- Sensory ataxia (finding) [SNOMED CT concept]
- Single limb ataxia (finding) [SNOMED CT concept]
- Tremor due to stroke [ICD-11 More detail]
- Truncal ataxia [HPO term]
- cerebellar disorders [MedlinePlus Topic]
- degenerative nerve diseases [MedlinePlus Topic]
- friedreich's ataxia [MedlinePlus Topic]
- motor ataxia [SNOMED Notion]
- movement disorders [MedlinePlus Topic]
- muscular incoordination [SNOMED Notion]
Currated CISMeF NLP mapping
- ATAXIA [WHO-ART High Level Term]
- Ataxia [PASCAL descriptor]
- Ataxia [MedDRA Preferred Term]
- Ataxia [NCIt concept]
- Ataxia [HPO term]
- Ataxia (finding) [SNOMED CT concept]
- Ataxia, unspecified [ICD-11 Subcategory]
- Coordination disturbance [MedDRA LLT]
- Coordination impaired [MedDRA LLT]
- Incoordination (finding) [SNOMED CT concept]
- Lack of coordination [ICD-11 Category]
- Lack of coordination [ICD-9 code]
- Trouble with Coordination [NCIt concept]
- ataxia [Disease (Nov.)]
- ataxia, nos [SNOMED Notion]
- coordination disorder, nos [SNOMED Notion]
- dyscoordination [Disease (Nov.)]
HPO term
- Dyssynergia [HPO term]
- Incoordination [HPO term]
- Limb ataxia [HPO term]
- Rubral tremor [HPO term]
- Sensory ataxia [HPO term]
- Truncal ataxia [HPO term]
MedlinePlus topic(s)
- degenerative nerve diseases [MedlinePlus Topic]
- friedreich's ataxia [MedlinePlus Topic]
- movement disorders [MedlinePlus Topic]
Record concept(s)
- ataxia [MeSH concept]
- ataxia, appendicular [MeSH concept]
- ataxia, motor [MeSH concept]
- ataxia, sensory [MeSH concept]
- ataxia, truncal [MeSH concept]
- dyscoordination [MeSH concept]
- tremor, rubral [MeSH concept]
Related MeSH Supplementary Concept(s)
- Ataxia-Microcephaly-Cataract syndrome [MeSH Supplementary Concept]
- Atonic-Astatic syndrome of foerster [MeSH Supplementary Concept]
- CANOMAD syndrome [MeSH Supplementary Concept]
- COACH syndrome [MeSH Supplementary Concept]
- Episodic Ataxia, Type 2 [MeSH Supplementary Concept]
- Richards-Rundle syndrome [MeSH Supplementary Concept]
- abetalipoproteinemia neuropathy [MeSH Supplementary Concept]
- arts syndrome [MeSH Supplementary Concept]
- ataxia and polyneuropathy, Adult-Onset [MeSH Supplementary Concept]
- ataxia with fasciculations [MeSH Supplementary Concept]
- ataxia with myoclonic epilepsy and presenile dementia [MeSH Supplementary Concept]
- ataxia with vitamin E deficiency [MeSH Supplementary Concept]
- ataxia, deafness, and cardiomyopathy [MeSH Supplementary Concept]
- ataxia, sensory, autosomal dominant [MeSH Supplementary Concept]
- ataxia, spastic, with congenital miosis [MeSH Supplementary Concept]
- bangstad syndrome [MeSH Supplementary Concept]
- behr syndrome [MeSH Supplementary Concept]
- bhaskar jagannathan syndrome [MeSH Supplementary Concept]
- carnitine acetyltransferase deficiency [MeSH Supplementary Concept]
- cataract ataxia deafness [MeSH Supplementary Concept]
- cataracts, ataxia, short stature, and mental retardation [MeSH Supplementary Concept]
- cerebral palsy, ataxic, autosomal recessive [MeSH Supplementary Concept]
- cerebroretinal microangiopathy with calcifications and cysts [MeSH Supplementary Concept]
- coenzyme Q10 deficiency [MeSH Supplementary Concept]
- deafness hyperuricemia neurologic ataxia [MeSH Supplementary Concept]
- diaminopentanuria [MeSH Supplementary Concept]
- episodic ataxia [MeSH Supplementary Concept]
- episodic ataxia, type 1 [MeSH Supplementary Concept]
- episodic ataxia, type 3 [MeSH Supplementary Concept]
- episodic ataxia, type 4 [MeSH Supplementary Concept]
- episodic ataxia, type 7 [MeSH Supplementary Concept]
- erythrokeratodermia with ataxia [MeSH Supplementary Concept]
- fragile X tremor ataxia syndrome [MeSH Supplementary Concept]
- hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response [MeSH Supplementary Concept]
- joubert syndrome 7 [MeSH Supplementary Concept]
- leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism [MeSH Supplementary Concept]
- mental retardation, X-Linked, syndromic, christianson type [MeSH Supplementary Concept]
- muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus [MeSH Supplementary Concept]
- myokymia 1 [MeSH Supplementary Concept]
- paroxysmal tonic upgaze, benign childhood, with ataxia [MeSH Supplementary Concept]
- partington X-linked mental retardation syndrome [MeSH Supplementary Concept]
- peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain [MeSH Supplementary Concept]
- polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract [MeSH Supplementary Concept]
- posterior column ataxia with retinitis pigmentosa [MeSH Supplementary Concept]
- reardon wilson cavanagh syndrome [MeSH Supplementary Concept]
- spastic paraplegia, ataxia, and mental retardation [MeSH Supplementary Concept]
- spondyloepimetaphyseal dysplasia, genevieve type [MeSH Supplementary Concept]
- tapetoretinal degeneration with ataxia [MeSH Supplementary Concept]
- treft sanborn carey syndrome [MeSH Supplementary Concept]
- tremor of intention, ataxia, and lipofuscinosis [MeSH Supplementary Concept]
- tryptophanuria with dwarfism [MeSH Supplementary Concept]
Semantic type(s)
- Sign or Symptom [UMLS semantic type]
UMLS correspondences (same concept)
- ATAXIA [WHO-ART High Level Term]
- Ataxia [MedDRA Preferred Term]
- Ataxia [NCIt concept]
- Ataxia (finding) [SNOMED CT concept]
- Ataxia, unspecified [ICD-10 Sub-category]
- Ataxia, unspecified [ICD-11 Subcategory]
- Dyssynergia [HPO term]
- ataxia, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Truncal ataxia (finding) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients