Ataxia

Codelist metadata

Coding system
SNOMED CT (UK Clinical Edition)
Coding system release
unknown
Author
Tom Nichols
Codelist ID
user/tom-nichols/ataxia
Version ID
7de5720e
Number of codes included
230
Download CSV Download definition

Versions

  1. 7de5720e Published
    Created: 21 Apr 2022 at 19:21
  2. 57c04d51 Published
    Created: 27 Mar 2022 at 20:39

About

No metadata has been provided for this codelist.

Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.

We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.

code term
1003847003 Pyruvate dehydrogenase phosphatase deficiency
1003849000 Pyruvate dehydrogenase complex E2 subunit deficiency
1003850000 Pyruvate dehydrogenase complex E1-alpha subunit deficiency
1003851001 Pyruvate dehydrogenase complex E1 beta subunit deficiency
10394003 Friedreich's ataxia
11145003 Single limb ataxia
129609000 Spinocerebellar ataxia
1767005 Fisher's syndrome
192871008 Early onset cerebellar ataxia with myoclonus
192874000 Cerebellar ataxia associated with another disorder
192877007 Paraneoplastic cerebellar degeneration
193165008 Neuropathy in association with hereditary ataxia
20262006 Ataxia
22443004 Vestibulocerebellar ataxia
230227009 Early onset cerebellar ataxia
230228004 Early onset cerebellar ataxia with retained tendon reflexes
230229007 Early onset cerebellar ataxia with hypogonadism
230230002 Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy
230231003 Early onset cerebellar ataxia with essential tremor
230232005 Late onset cerebellar ataxia
230233000 Progressive cerebellar ataxia
230234006 Periodic ataxia
230235007 Olivopontocerebellar atrophy with slow eye movement
230236008 Olivopontocerebellar atrophy with blindness
230237004 Progressive spinocerebellar ataxia with decreased tendon reflexes
230238009 Progressive spinocerebellar ataxia with retained tendon reflexes
230239001 Progressive cerebellar ataxia with palatal myoclonus
230240004 Progressive cerebellar ataxia with hypogonadism
230242007 Drug-induced cerebellar ataxia
230243002 Cerebellar ataxia caused by toxin
231509001 Dissociative astasia-abasia
237611007 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
237614004 Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency
237984008 Neurogenic muscle weakness, ataxia and retinitis pigmentosa
24059009 Acute cerebellar ataxia caused by varicella
246767003 Abnormal saccadic eye movement
250048009 Frontal ataxia
250053004 Parkinsonian ataxia
250062002 Arms ataxic
250065000 Legs ataxic
250067008 Truncal ataxia
253176002 Gillespie syndrome
25362006 Phytanic acid storage disease
254092004 Saldino-Mainzer dysplasia
278509004 Congenital non-progressive ataxia
278512001 Ataxic cerebral palsy
28634005 Cerebral ataxia
290581000119101 Ataxia due to and following cerebrovascular accident
29941000119105 Ataxia as sequela of cerebrovascular disease
29951000119107 Ataxic hemiparesis
300992002 Alcohol-induced cerebellar ataxia
314840009 Progressive locomotor ataxia
32680009 Nothnagel's syndrome
361272001 Cerebellar ataxia due to alcoholism
371313002 Congenital cerebellar cortical atrophy
3756000 Static ataxia
37960002 Sanger-Brown cerebellar ataxia
40259002 Progressive sensory ataxia of Charolais
420932006 Episodic ataxia type 2
421182009 Episodic ataxia type 1
421455009 Episodic ataxia
425219008 Progressive spinal ataxia
43977004 Corticostriatal-spinal degeneration
444980006 Sporadic olivopontocerebellar atrophy
445458007 Sensory ataxia
448045004 Fragile X associated tremor ataxia syndrome
450881007 Hypermetria
45853006 Roussy-Lévy syndrome
45897005 Jervis' syndrome
46683007 Pyruvate dehydrogenase complex deficiency
46808003 Marie's cerebellar ataxia
5822000 Athetosis with spastic paraplegia
59103002 Cerebral paralysis with homolateral ataxia
59546009 Motor ataxia
60146005 Bailey-Cushing syndrome
60935008 Paramyoclonus multiplex
674111000119100 Ataxia due to and following ischemic cerebrovascular accident
674121000119107 Ataxia due to and following hemorrhagic cerebrovascular accident
67761004 Olivopontocerebellar degeneration
68107009 Cerebral paresis with homolateral ataxia
68116008 Dentatorubropallidoluysian degeneration
68504005 Ataxia-telangiectasia syndrome
690201000119109 Ataxia due to and following embolic cerebrovascular accident
69131009 Spinal ataxia
69752006 Hypometria
698036008 Oral motor ataxia
699328003 Myoclonic epilepsy myopathy sensory ataxia
700058006 Ataxia-telangiectasia-like disorder
702326000 Progressive myoclonus epilepsy with ataxia
702441001 Fatal X-linked ataxia with deafness and loss of vision
702442008 Ataxia with vitamin E deficiency
702445005 Autosomal recessive spastic ataxia of Charlevoix-Saguenay
711158005 Spinocerebellar ataxia type 36
711412004 3-methylglutaconic aciduria type 5
715366004 Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
715369006 Autosomal recessive cerebelloparenchymal disorder type 3
715371006 Cerebellar ataxia co-occurrent with ectodermal dysplasia
715415005 Richards-Rundle syndrome
715465001 Spinocerebellar degeneration co-occurrent with macular corneal dystrophy
715483009 Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss
715564000 Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity
715726000 Spinocerebellar ataxia type 7
715748006 Spinocerebellar ataxia type 1
715751004 Spinocerebellar ataxia type 2
715752006 Spinocerebellar ataxia type 6
715753001 Spinocerebellar ataxia type 8
715754007 Spinocerebellar ataxia type 10
715755008 Spinocerebellar ataxia type 4
715776003 Spastic paraplegia type 7
715824008 Spinocerebellar ataxia type 28
715825009 Spinocerebellar ataxia type 29
715826005 Spinocerebellar ataxia type 31
715984007 Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome
716724006 Spinocerebellar ataxia type 15/16
717266001 Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome
717332007 Cerebellar ataxia Cayman type
71802006 Astasia-abasia
718752007 Episodic ataxia type 7
718753002 Episodic ataxia type 6
718754008 Episodic ataxia type 4
718755009 Episodic ataxia type 3
718756005 Episodic ataxia type 5
718769009 Spinocerebellar ataxia type 26
718770005 Spinocerebellar ataxia type 25
718771009 Spinocerebellar ataxia type 20
718772002 Spinocerebellar ataxia type 23
718774001 Spinocerebellar ataxia type 21
718845002 X-linked intellectual disability with ataxia and apraxia syndrome
719102004 Congenital cataract with ataxia and deafness syndrome
719207000 Spinocerebellar ataxia type 11
719208005 Spinocerebellar ataxia type 12
719209002 Spinocerebellar ataxia type 13
719210007 Spinocerebellar ataxia type 14
719249005 Spinocerebellar ataxia type 17
719250005 Spinocerebellar ataxia type 18
719251009 Spinocerebellar ataxia type 19
719252002 Spinocerebellar ataxia type 27
719253007 Spinocerebellar ataxia type 30
719254001 Spinocerebellar ataxia type 32
719255000 Spinocerebellar ataxia type 34
719300001 Spinocerebellar ataxia type 35
719301002 Spinocerebellar ataxia type 37
719302009 Spinocerebellar ataxia type 5
719816006 X-linked sideroblastic anemia with spinocerebellar ataxia
719817002 X-linked spinocerebellar ataxia type 3
719818007 X-linked spinocerebellar ataxia type 4
720517001 Ataxia with deafness and intellectual disability syndrome
720634003 Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
720750004 Spinocerebellar degeneration and corneal dystrophy syndrome
721207002 Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome
721847002 Joubert syndrome with congenital hepatic fibrosis
722293005 Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
722967008 Ataxia due to mitochondrial mutations
722968003 Acquired ataxia
723441001 Non-progressive cerebellar ataxia with intellectual disability
723452007 Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
724065003 Autosomal recessive posterior column ataxia and retinitis pigmentosa
724227000 Infantile onset spinocerebellar ataxia
724283004 Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
724765008 Chorea co-occurrent and due to dentatorubropallidoluysian degeneration
724768005 Ataxia co-occurrent and due to cerebrotendinous xanthomatosis
724769002 Ataxia co-occurrent and due to phytanic acid storage disease
724770001 Ataxia co-occurrent and due to abetalipoproteinemia
725394006 Autosomal recessive ataxia due to ubiquinone deficiency
725408001 Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
725433003 Autosomal recessive cerebellar ataxia Beauce type
726031001 Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome
73119000 Retinitis pigmentosa-deafness-ataxia syndrome
733033001 Spinocerebellar ataxia dysmorphism syndrome
733065003 Myoclonus, cerebellar ataxia, deafness syndrome
734020000 Spinocerebellar ataxia type 40
734021001 Spinocerebellar ataxia type 38
734023003 Sporadic adult-onset ataxia of unknown etiology
73495003 Dyssynergia cerebellaris myoclonica
763065008 Ataxia telangiectasia variant
763127004 Benign paroxysmal tonic upgaze of childhood with ataxia
763312008 Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
763344007 Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
763348005 Autosomal recessive cerebellar ataxia with late-onset spasticity
763351003 Spectrin-associated autosomal recessive cerebellar ataxia
763597000 Hereditary ataxia
763669001 Spastic ataxia with congenital miosis
764095005 Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome
765089003 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome
765091006 Spinocerebellar ataxia with axonal neuropathy type 1
765212008 Balint syndrome
766814006 Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
766818009 X-linked non progressive cerebellar ataxia
768556005 Ataxia pancytopenia syndrome
768663003 Leukoencephalopathy with mild cerebellar ataxia and white matter edema
770720005 Autosomal recessive spastic paraplegia type 58
770898002 Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency
771271000 Steroid-responsive encephalopathy associated with autoimmune thyroiditis
771469002 Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome
771514002 Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome
773492007 Childhood-onset spasticity with hyperglycinemia
773495009 Episodic ataxia with slurred speech
773498006 Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency
773769008 Ataxia, photosensitivity, short stature syndrome
782690007 Gemignani syndrome
782696001 Recessive mitochondrial ataxia syndrome
782719004 Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency
782721009 Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency
782753000 Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome
783060009 Autosomal recessive cerebellar ataxia, psychomotor delay syndrome
783062001 Progressive myoclonic epilepsy type 6
783203003 Ataxia with tapetoretinal degeneration syndrome
784343003 Autosomal recessive spastic ataxia with leukoencephalopathy
784347002 Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
784380009 Autosomal dominant spastic ataxia type 1
785300001 Infantile-onset autosomal recessive non progressive cerebellar ataxia
785301002 Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
785302009 Adult-onset autosomal recessive cerebellar ataxia
787174003 Intellectual disability, hyperkinetic movement, truncal ataxia syndrome
789657008 ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
79161002 Ocular dysmetria
80734006 Marinesco-Sjögren syndrome
827172005 X-linked progressive cerebellar ataxia
830119000 Ataxia of bilateral lower limbs
830120006 Ataxia of bilateral upper limbs
838331007 Ataxia due to chronic infection of central nervous system
85102008 Cerebellar ataxia
87694001 Pyruvate carboxylase deficiency
90791004 Posthemiplegic ataxia
91502009 Spinocerebellar disease
91952008 Azorean disease
91953003 Azorean disease, type I
91954009 Azorean disease, type II
91955005 Azorean disease, type III
91956006 Azorean disease, type IV

This page shows the search terms that were used to build the codelist. Concepts that match the search terms, but which were excluded, are in faint grey.

Ataxia (finding)

Included 179 out of 182 matching concepts.

Show matching concepts
  • ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis (789657008)
  • Acquired ataxia (722968003)
  • Acute cerebellar ataxia caused by varicella (24059009)
  • Adult-onset autosomal recessive cerebellar ataxia (785302009)
  • Alcohol-induced cerebellar ataxia (300992002)
  • Arms ataxic (250062002)
  • Ataxia (20262006)
  • Ataxia as sequela of cerebrovascular disease (29941000119105)
  • Ataxia co-occurrent and due to abetalipoproteinemia (724770001)
  • Ataxia co-occurrent and due to cerebrotendinous xanthomatosis (724768005)
  • Ataxia co-occurrent and due to phytanic acid storage disease (724769002)
  • Ataxia due to and following cerebrovascular accident (290581000119101)
  • Ataxia due to and following embolic cerebrovascular accident (690201000119109)
  • Ataxia due to and following hemorrhagic cerebrovascular accident (674121000119107)
  • Ataxia due to and following ischemic cerebrovascular accident (674111000119100)
  • Ataxia due to chronic infection of central nervous system (838331007)
  • Ataxia due to mitochondrial mutations (722967008)
  • Ataxia of bilateral lower limbs (830119000)
  • Ataxia of bilateral upper limbs (830120006)
  • Ataxia pancytopenia syndrome (768556005)
  • Ataxia with deafness and intellectual disability syndrome (720517001)
  • Ataxia with tapetoretinal degeneration syndrome (783203003)
  • Ataxia, photosensitivity, short stature syndrome (773769008)
  • Ataxic cerebral palsy (278512001)
  • Ataxic hemiparesis (29951000119107)
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (722293005)
  • Autosomal dominant spastic ataxia type 1 (784380009)
  • Autosomal recessive ataxia due to ubiquinone deficiency (725394006)
  • Autosomal recessive cerebellar ataxia Beauce type (725433003)
  • Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency (782719004)
  • Autosomal recessive cerebellar ataxia with late-onset spasticity (763348005)
  • Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (715366004)
  • Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (725408001)
  • Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome (766814006)
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (782721009)
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (773498006)
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (770898002)
  • Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (783060009)
  • Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (763312008)
  • Autosomal recessive cerebelloparenchymal disorder type 3 (715369006)
  • Autosomal recessive posterior column ataxia and retinitis pigmentosa (724065003)
  • Autosomal recessive spastic ataxia of Charlevoix-Saguenay (702445005)
  • Autosomal recessive spastic ataxia with leukoencephalopathy (784343003)
  • Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome (784347002)
  • Azorean disease (91952008)
  • Azorean disease, type I (91953003)
  • Azorean disease, type II (91954009)
  • Azorean disease, type III (91955005)
  • Azorean disease, type IV (91956006)
  • Cerebellar ataxia (85102008)
  • Cerebellar ataxia Cayman type (717332007)
  • Cerebellar ataxia associated with another disorder (192874000)
  • Cerebellar ataxia caused by toxin (230243002)
  • Cerebellar ataxia co-occurrent with ectodermal dysplasia (715371006)
  • Cerebellar ataxia due to alcoholism (361272001)
  • Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (715984007)
  • Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome (720634003)
  • Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (763344007)
  • Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (726031001)
  • Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (785301002)
  • Childhood-onset spasticity with hyperglycinemia (773492007)
  • Chorea co-occurrent and due to dentatorubropallidoluysian degeneration (724765008)
  • Congenital cataract with ataxia and deafness syndrome (719102004)
  • Congenital non-progressive ataxia (278509004)
  • Dentatorubropallidoluysian degeneration (68116008)
  • Drug-induced cerebellar ataxia (230242007)
  • Dyssynergia cerebellaris myoclonica (73495003)
  • Early onset cerebellar ataxia (230227009)
  • Early onset cerebellar ataxia with essential tremor (230231003)
  • Early onset cerebellar ataxia with hypogonadism (230229007)
  • Early onset cerebellar ataxia with myoclonus (192871008)
  • Early onset cerebellar ataxia with retained tendon reflexes (230228004)
  • Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy (230230002)
  • Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (771514002)
  • Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (771469002)
  • Episodic ataxia (421455009)
  • Episodic ataxia type 1 (421182009)
  • Episodic ataxia type 2 (420932006)
  • Episodic ataxia type 3 (718755009)
  • Episodic ataxia type 4 (718754008)
  • Episodic ataxia type 5 (718756005)
  • Episodic ataxia type 6 (718753002)
  • Episodic ataxia type 7 (718752007)
  • Episodic ataxia with slurred speech (773495009)
  • Fatal X-linked ataxia with deafness and loss of vision (702441001)
  • Fragile X associated tremor ataxia syndrome (448045004)
  • Frontal ataxia (250048009)
  • Gemignani syndrome (782690007)
  • Gillespie syndrome (253176002)
  • Hereditary ataxia (763597000)
  • Hypermetria (450881007)
  • Hypometria (69752006)
  • Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (724283004)
  • Infantile onset spinocerebellar ataxia (724227000)
  • Infantile-onset autosomal recessive non progressive cerebellar ataxia (785300001)
  • Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (782753000)
  • Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (787174003)
  • Late onset cerebellar ataxia (230232005)
  • Legs ataxic (250065000)
  • Leukoencephalopathy with mild cerebellar ataxia and white matter edema (768663003)
  • Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (764095005)
  • Marie's cerebellar ataxia (46808003)
  • Marinesco-Sjögren syndrome (80734006)
  • Motor ataxia (59546009)
  • Myoclonus, cerebellar ataxia, deafness syndrome (733065003)
  • Neuropathy in association with hereditary ataxia (193165008)
  • Non-progressive cerebellar ataxia with intellectual disability (723441001)
  • Nothnagel's syndrome (32680009)
  • Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (715483009)
  • Olivopontocerebellar atrophy with blindness (230236008)
  • Olivopontocerebellar atrophy with slow eye movement (230235007)
  • Olivopontocerebellar degeneration (67761004)
  • On examination - arms ataxic (163768005)
  • On examination - ataxia (275858008)
  • On examination - legs ataxic (163769002)
  • Oral motor ataxia (698036008)
  • Parkinsonian ataxia (250053004)
  • Periodic ataxia (230234006)
  • Progressive cerebellar ataxia (230233000)
  • Progressive cerebellar ataxia with hypogonadism (230240004)
  • Progressive cerebellar ataxia with palatal myoclonus (230239001)
  • Progressive spinocerebellar ataxia with decreased tendon reflexes (230237004)
  • Progressive spinocerebellar ataxia with retained tendon reflexes (230238009)
  • Recessive mitochondrial ataxia syndrome (782696001)
  • Richards-Rundle syndrome (715415005)
  • Saldino-Mainzer dysplasia (254092004)
  • Sanger-Brown cerebellar ataxia (37960002)
  • Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (721207002)
  • Sensory ataxia (445458007)
  • Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome (717266001)
  • Single limb ataxia (11145003)
  • Spastic ataxia with congenital miosis (763669001)
  • Spastic paraplegia type 7 (715776003)
  • Spectrin-associated autosomal recessive cerebellar ataxia (763351003)
  • Spinocerebellar ataxia (129609000)
  • Spinocerebellar ataxia dysmorphism syndrome (733033001)
  • Spinocerebellar ataxia type 1 (715748006)
  • Spinocerebellar ataxia type 10 (715754007)
  • Spinocerebellar ataxia type 11 (719207000)
  • Spinocerebellar ataxia type 12 (719208005)
  • Spinocerebellar ataxia type 13 (719209002)
  • Spinocerebellar ataxia type 14 (719210007)
  • Spinocerebellar ataxia type 15/16 (716724006)
  • Spinocerebellar ataxia type 17 (719249005)
  • Spinocerebellar ataxia type 18 (719250005)
  • Spinocerebellar ataxia type 19 (719251009)
  • Spinocerebellar ataxia type 2 (715751004)
  • Spinocerebellar ataxia type 20 (718771009)
  • Spinocerebellar ataxia type 21 (718774001)
  • Spinocerebellar ataxia type 23 (718772002)
  • Spinocerebellar ataxia type 25 (718770005)
  • Spinocerebellar ataxia type 26 (718769009)
  • Spinocerebellar ataxia type 27 (719252002)
  • Spinocerebellar ataxia type 28 (715824008)
  • Spinocerebellar ataxia type 29 (715825009)
  • Spinocerebellar ataxia type 30 (719253007)
  • Spinocerebellar ataxia type 31 (715826005)
  • Spinocerebellar ataxia type 32 (719254001)
  • Spinocerebellar ataxia type 34 (719255000)
  • Spinocerebellar ataxia type 35 (719300001)
  • Spinocerebellar ataxia type 36 (711158005)
  • Spinocerebellar ataxia type 37 (719301002)
  • Spinocerebellar ataxia type 38 (734021001)
  • Spinocerebellar ataxia type 4 (715755008)
  • Spinocerebellar ataxia type 40 (734020000)
  • Spinocerebellar ataxia type 5 (719302009)
  • Spinocerebellar ataxia type 6 (715752006)
  • Spinocerebellar ataxia type 7 (715726000)
  • Spinocerebellar ataxia type 8 (715753001)
  • Spinocerebellar ataxia with axonal neuropathy type 1 (765091006)
  • Spinocerebellar degeneration and corneal dystrophy syndrome (720750004)
  • Sporadic adult-onset ataxia of unknown etiology (734023003)
  • Sporadic olivopontocerebellar atrophy (444980006)
  • Static ataxia (3756000)
  • Steroid-responsive encephalopathy associated with autoimmune thyroiditis (771271000)
  • Truncal ataxia (250067008)
  • X-linked intellectual disability with ataxia and apraxia syndrome (718845002)
  • X-linked non progressive cerebellar ataxia (766818009)
  • X-linked progressive cerebellar ataxia (827172005)
  • X-linked sideroblastic anemia with spinocerebellar ataxia (719816006)
  • X-linked spinocerebellar ataxia type 3 (719817002)
  • X-linked spinocerebellar ataxia type 4 (719818007)

ataxia

Included 224 out of 276 matching concepts.

Show matching concepts
  • (Cerebellar ataxia NOS) or (Roussy-Levy syndrome) (192873006)
  • (Hysterical aphonia) or (hysterical ataxia) or (Ganser's syndrome) or (hysteria NOS) (191719007)
  • (Spinocerebellar disease) or (cerebellar ataxia) or (cerebellar disease) (267691001)
  • (Spinocerebellar disease) or (cerebellar ataxia) or (cerebellar disease) (155010002)
  • (Syphilitic: [tabes dorsalis] or [spinal sclerosis]) or (locomotor ataxia) (186885003)
  • 3-methylglutaconic aciduria type 5 (711412004)
  • ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis (789657008)
  • Abnormal saccadic eye movement (246767003)
  • Abortive cerebellar ataxia (66988006)
  • Acquired ataxia (722968003)
  • Acute cerebellar ataxia caused by varicella (24059009)
  • Adult-onset autosomal recessive cerebellar ataxia (785302009)
  • Alcohol-induced cerebellar ataxia (300992002)
  • Arms ataxic (250062002)
  • Assessment using Scale for Assessment and Rating of Ataxia (865930008)
  • Astasia-abasia (71802006)
  • Ataxia (20262006)
  • Ataxia [D] (158202006)
  • Ataxia as sequela of cerebrovascular disease (29941000119105)
  • Ataxia co-occurrent and due to abetalipoproteinemia (724770001)
  • Ataxia co-occurrent and due to cerebrotendinous xanthomatosis (724768005)
  • Ataxia co-occurrent and due to phytanic acid storage disease (724769002)
  • Ataxia due to and following cerebrovascular accident (290581000119101)
  • Ataxia due to and following embolic cerebrovascular accident (690201000119109)
  • Ataxia due to and following hemorrhagic cerebrovascular accident (674121000119107)
  • Ataxia due to and following ischemic cerebrovascular accident (674111000119100)
  • Ataxia due to chronic infection of central nervous system (838331007)
  • Ataxia due to mitochondrial mutations (722967008)
  • Ataxia of bilateral lower limbs (830119000)
  • Ataxia of bilateral upper limbs (830120006)
  • Ataxia pancytopenia syndrome (768556005)
  • Ataxia telangiectasia variant (763065008)
  • Ataxia with deafness and intellectual disability syndrome (720517001)
  • Ataxia with tapetoretinal degeneration syndrome (783203003)
  • Ataxia with vitamin E deficiency (702442008)
  • Ataxia, photosensitivity, short stature syndrome (773769008)
  • Ataxia-telangiectasia syndrome (68504005)
  • Ataxia-telangiectasia-like disorder (700058006)
  • Ataxic cerebral palsy (278512001)
  • Ataxic hemiparesis (29951000119107)
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (722293005)
  • Autosomal dominant spastic ataxia type 1 (784380009)
  • Autosomal recessive ataxia due to ubiquinone deficiency (725394006)
  • Autosomal recessive cerebellar ataxia Beauce type (725433003)
  • Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency (782719004)
  • Autosomal recessive cerebellar ataxia with late-onset spasticity (763348005)
  • Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (715366004)
  • Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (725408001)
  • Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome (766814006)
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (782721009)
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (773498006)
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (770898002)
  • Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (783060009)
  • Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (763312008)
  • Autosomal recessive cerebelloparenchymal disorder type 3 (715369006)
  • Autosomal recessive posterior column ataxia and retinitis pigmentosa (724065003)
  • Autosomal recessive spastic ataxia of Charlevoix-Saguenay (702445005)
  • Autosomal recessive spastic ataxia with leukoencephalopathy (784343003)
  • Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome (784347002)
  • Autosomal recessive spastic paraplegia type 58 (770720005)
  • Azorean disease (91952008)
  • Azorean disease, type I (91953003)
  • Azorean disease, type II (91954009)
  • Azorean disease, type III (91955005)
  • Azorean disease, type IV (91956006)
  • Balint syndrome (765212008)
  • Benign paroxysmal tonic upgaze of childhood with ataxia (763127004)
  • Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency (237614004)
  • Cardiomyopathy in Friedreich's ataxia (195030007)
  • Cerebellar ataxia (85102008)
  • Cerebellar ataxia Cayman type (717332007)
  • Cerebellar ataxia NOS (155012005)
  • Cerebellar ataxia NOS (685011000000101)
  • Cerebellar ataxia NOS (267586009)
  • Cerebellar ataxia associated with another disorder (192874000)
  • Cerebellar ataxia caused by toxin (230243002)
  • Cerebellar ataxia co-occurrent with ectodermal dysplasia (715371006)
  • Cerebellar ataxia due to alcoholism (361272001)
  • Cerebellar ataxia in disease NOS (192878002)
  • Cerebellar ataxia in disease NOS (583071000000104)
  • Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (715984007)
  • Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome (720634003)
  • Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (763344007)
  • Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (726031001)
  • Cerebral ataxia (28634005)
  • Cerebral ataxia (192822003)
  • Cerebral paralysis with homolateral ataxia (59103002)
  • Cerebral paresis with homolateral ataxia (68107009)
  • Cervical malformation - malarticulation (77858006)
  • Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (785301002)
  • Childhood-onset spasticity with hyperglycinemia (773492007)
  • Chorea co-occurrent and due to dentatorubropallidoluysian degeneration (724765008)
  • Congenital cataract with ataxia and deafness syndrome (719102004)
  • Congenital cerebellar cortical atrophy (16954003)
  • Congenital cerebellar cortical atrophy (371313002)
  • Congenital non-progressive ataxia (192879005)
  • Congenital non-progressive ataxia (278509004)
  • Dentatorubropallidoluysian degeneration (68116008)
  • Dilated cardiomyopathy secondary to Friedreich's ataxia (50270004)
  • Dissociative astasia-abasia (231509001)
  • Drug-induced cerebellar ataxia (230242007)
  • Dyssynergia cerebellaris myoclonica (73495003)
  • Early onset cerebellar ataxia (230227009)
  • Early onset cerebellar ataxia with essential tremor (230231003)
  • Early onset cerebellar ataxia with hypogonadism (230229007)
  • Early onset cerebellar ataxia with hypogonadism (808431000000103)
  • Early onset cerebellar ataxia with myoclonus (192871008)
  • Early onset cerebellar ataxia with retained tendon reflexes (230228004)
  • Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy (230230002)
  • Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (771514002)
  • Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (771469002)
  • Epilepsy, ataxia, sensorineural deafness and tubulopathy syndrome (887101000000101)
  • Epilepsy, ataxia, sensorineural deafness, and tubulopathy syndrome (700448000)
  • Episodic ataxia (421455009)
  • Episodic ataxia type 1 (421182009)
  • Episodic ataxia type 2 (420932006)
  • Episodic ataxia type 3 (718755009)
  • Episodic ataxia type 4 (718754008)
  • Episodic ataxia type 5 (718756005)
  • Episodic ataxia type 6 (718753002)
  • Episodic ataxia type 7 (718752007)
  • Episodic ataxia with slurred speech (773495009)
  • Family history of spinocerebellar ataxia (63881000119101)
  • Fatal X-linked ataxia with deafness and loss of vision (702441001)
  • Fisher's syndrome (1767005)
  • Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (765089003)
  • Fragile X associated tremor ataxia syndrome (759431000000104)
  • Fragile X associated tremor ataxia syndrome (830921000000101)
  • Fragile X associated tremor ataxia syndrome (448045004)
  • Friedreich ataxia (155011003)
  • Friedreich's ataxia (10394003)
  • Frontal ataxia (250048009)
  • Gemignani syndrome (782690007)
  • Germline whole genome sequencing targeting adult onset hereditary ataxia panel (63021000000100)
  • Germline whole genome sequencing targeting adult onset hereditary ataxia panel for adult onset hereditary ataxia (82501000000106)
  • Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (63051000000105)
  • Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for cerebellar anomalies (63381000000102)
  • Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for childhood onset hereditary ataxia (63361000000106)
  • Gillespie syndrome (253176002)
  • Hereditary ataxia (763597000)
  • Hereditary ataxia in Terriers (12057006)
  • Hypermetria (450881007)
  • Hypertrophic cardiomyopathy due to Friedreich ataxia (890119003)
  • Hypertrophic cardiomyopathy secondary to Friedreich's ataxia (53322007)
  • Hypometria (69752006)
  • Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (724283004)
  • Infantile onset spinocerebellar ataxia (724227000)
  • Infantile-onset autosomal recessive non progressive cerebellar ataxia (785300001)
  • Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (782753000)
  • Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (787174003)
  • Joubert syndrome with congenital hepatic fibrosis (721847002)
  • Late onset cerebellar ataxia (230232005)
  • Legs ataxic (250065000)
  • Leukoencephalopathy with mild cerebellar ataxia and white matter edema (768663003)
  • Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (764095005)
  • Marie's cerebellar ataxia (192869008)
  • Marie's cerebellar ataxia (393576001)
  • Marie's cerebellar ataxia (46808003)
  • Marinesco-Sjögren syndrome (80734006)
  • Motor ataxia (59546009)
  • Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus (237611007)
  • Myoclonic epilepsy myopathy sensory ataxia (699328003)
  • Myoclonus, cerebellar ataxia, deafness syndrome (733065003)
  • Neurogenic muscle weakness, ataxia and retinitis pigmentosa (237984008)
  • Neuropathy in association with hereditary ataxia (193165008)
  • Non-progressive cerebellar ataxia with intellectual disability (723441001)
  • Nothnagel's syndrome (32680009)
  • O/E: [coordination] or [Romberg's test] or [ataxia] (140967004)
  • O/E: [coordination] or [Romberg's test] or [ataxia] (163766009)
  • Ocular dysmetria (79161002)
  • Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (715483009)
  • Olivopontocerebellar atrophy with blindness (230236008)
  • Olivopontocerebellar atrophy with slow eye movement (230235007)
  • Olivopontocerebellar degeneration (67761004)
  • On examination - arms ataxic (163768005)
  • On examination - ataxia (275858008)
  • On examination - legs ataxic (163769002)
  • Oral motor ataxia (698036008)
  • Paraneoplastic cerebellar degeneration (192877007)
  • Parkinsonian ataxia (250053004)
  • Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (715564000)
  • Periodic ataxia (230234006)
  • Phytanic acid storage disease (25362006)
  • Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (723452007)
  • Posthemiplegic ataxia (90791004)
  • Progressive cerebellar ataxia (230233000)
  • Progressive cerebellar ataxia with hypogonadism (230240004)
  • Progressive cerebellar ataxia with palatal myoclonus (230239001)
  • Progressive locomotor ataxia (314840009)
  • Progressive myoclonic epilepsy type 6 (783062001)
  • Progressive myoclonus epilepsy with ataxia (702326000)
  • Progressive sensory ataxia of Charolais (40259002)
  • Progressive spinal ataxia (425219008)
  • Progressive spinocerebellar ataxia with decreased tendon reflexes (230237004)
  • Progressive spinocerebellar ataxia with retained tendon reflexes (230238009)
  • Proximal tubulopathy, diabetes mellitus, cerebellar ataxia syndrome (724062000)
  • Pyruvate carboxylase deficiency (87694001)
  • Pyruvate dehydrogenase complex E1 beta subunit deficiency (1003851001)
  • Pyruvate dehydrogenase complex E1-alpha subunit deficiency (1003850000)
  • Pyruvate dehydrogenase complex E2 subunit deficiency (1003849000)
  • Pyruvate dehydrogenase complex deficiency (46683007)
  • Pyruvate dehydrogenase phosphatase deficiency (1003847003)
  • Recessive mitochondrial ataxia syndrome (782696001)
  • Retinitis pigmentosa-deafness-ataxia syndrome (73119000)
  • Richards-Rundle syndrome (715415005)
  • Roussy-Lévy syndrome (45853006)
  • Saldino-Mainzer dysplasia (254092004)
  • Sanger-Brown cerebellar ataxia (192870009)
  • Sanger-Brown cerebellar ataxia (37960002)
  • Scale for Assessment and Rating of Ataxia (865931007)
  • Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (721207002)
  • Sensory ataxia (445458007)
  • Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome (717266001)
  • Single limb ataxia (11145003)
  • Spastic ataxia with congenital miosis (763669001)
  • Spastic paraplegia type 7 (715776003)
  • Spectrin-associated autosomal recessive cerebellar ataxia (763351003)
  • Spinal ataxia (69131009)
  • Spinocerebellar ataxia (129609000)
  • Spinocerebellar ataxia dysmorphism syndrome (733033001)
  • Spinocerebellar ataxia type 1 (715748006)
  • Spinocerebellar ataxia type 10 (715754007)
  • Spinocerebellar ataxia type 11 (719207000)
  • Spinocerebellar ataxia type 12 (719208005)
  • Spinocerebellar ataxia type 13 (719209002)
  • Spinocerebellar ataxia type 14 (719210007)
  • Spinocerebellar ataxia type 15/16 (716724006)
  • Spinocerebellar ataxia type 17 (719249005)
  • Spinocerebellar ataxia type 18 (719250005)
  • Spinocerebellar ataxia type 19 (719251009)
  • Spinocerebellar ataxia type 2 (715751004)
  • Spinocerebellar ataxia type 20 (718771009)
  • Spinocerebellar ataxia type 21 (718774001)
  • Spinocerebellar ataxia type 23 (718772002)
  • Spinocerebellar ataxia type 25 (718770005)
  • Spinocerebellar ataxia type 26 (718769009)
  • Spinocerebellar ataxia type 27 (719252002)
  • Spinocerebellar ataxia type 28 (715824008)
  • Spinocerebellar ataxia type 29 (715825009)
  • Spinocerebellar ataxia type 30 (719253007)
  • Spinocerebellar ataxia type 31 (715826005)
  • Spinocerebellar ataxia type 32 (719254001)
  • Spinocerebellar ataxia type 34 (719255000)
  • Spinocerebellar ataxia type 35 (719300001)
  • Spinocerebellar ataxia type 36 (711158005)
  • Spinocerebellar ataxia type 37 (719301002)
  • Spinocerebellar ataxia type 38 (734021001)
  • Spinocerebellar ataxia type 4 (715755008)
  • Spinocerebellar ataxia type 40 (734020000)
  • Spinocerebellar ataxia type 5 (719302009)
  • Spinocerebellar ataxia type 6 (715752006)
  • Spinocerebellar ataxia type 7 (715726000)
  • Spinocerebellar ataxia type 8 (715753001)
  • Spinocerebellar ataxia with axonal neuropathy type 1 (765091006)
  • Spinocerebellar degeneration and corneal dystrophy syndrome (720750004)
  • Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (715465001)
  • Sporadic adult-onset ataxia of unknown etiology (734023003)
  • Sporadic olivopontocerebellar atrophy (444980006)
  • Static ataxia (3756000)
  • Steroid-responsive encephalopathy associated with autoimmune thyroiditis (771271000)
  • Swayback of sheep (78714004)
  • Tremorgenataxia syndrome (33433001)
  • Truncal ataxia (250067008)
  • Vestibulocerebellar ataxia (22443004)
  • X-linked intellectual disability with ataxia and apraxia syndrome (718845002)
  • X-linked non progressive cerebellar ataxia (766818009)
  • X-linked progressive cerebellar ataxia (827172005)
  • X-linked sideroblastic anemia with spinocerebellar ataxia (719816006)
  • X-linked spinocerebellar ataxia type 3 (719817002)
  • X-linked spinocerebellar ataxia type 4 (719818007)
  • [D]Ataxia (502251000000105)
  • [D]Ataxia (274241003)
  • [D]Ataxia NOS (206825002)
  • [D]Ataxia NOS (450391000000109)
  • [X]Other hereditary ataxias (194460000)
  • [X]Other hereditary ataxias (431951000000108)

ataxia telangectasia

Included 0 out of 0 matching concepts.

Show matching concepts

spinocerebellar disease

Included 70 out of 81 matching concepts.

Show matching concepts
  • (Hereditary spastic paraplegia) or (spinicerebellar disease NOS) (155013000)
  • (Hereditary spastic paraplegia) or (spinicerebellar disease NOS) (267692008)
  • (Spinocerebellar disease) or (cerebellar ataxia) or (cerebellar disease) (267691001)
  • (Spinocerebellar disease) or (cerebellar ataxia) or (cerebellar disease) (155010002)
  • ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis (789657008)
  • Adult-onset autosomal recessive cerebellar ataxia (785302009)
  • Ataxia-telangiectasia syndrome (68504005)
  • Athetosis with spastic paraplegia (5822000)
  • Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency (782719004)
  • Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (782721009)
  • Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (783060009)
  • Autosomal recessive cerebelloparenchymal disorder type 3 (715369006)
  • Azorean disease (91952008)
  • Azorean disease, type I (91953003)
  • Azorean disease, type II (91954009)
  • Azorean disease, type III (91955005)
  • Azorean disease, type IV (91956006)
  • Bailey-Cushing syndrome (60146005)
  • Cerebellar &/or spinocerebellar disease (192867005)
  • Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (785301002)
  • Corticostriatal-spinal degeneration (43977004)
  • Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (771469002)
  • Friedreich's ataxia (10394003)
  • Infantile onset spinocerebellar ataxia (724227000)
  • Jervis' syndrome (45897005)
  • Myoclonic epilepsy myopathy sensory ataxia (699328003)
  • Nothnagel's syndrome (32680009)
  • Other spinocerebellar disease NOS (646131000000107)
  • Other spinocerebellar disease NOS (192882000)
  • Other spinocerebellar diseases (192880008)
  • Other spinocerebellar diseases (630441000000109)
  • Paramyoclonus multiplex (60935008)
  • Posthemiplegic ataxia (90791004)
  • Progressive spinocerebellar ataxia with retained tendon reflexes (230238009)
  • Richards-Rundle syndrome (715415005)
  • Sanger-Brown cerebellar ataxia (37960002)
  • Spinocerebellar ataxia (129609000)
  • Spinocerebellar ataxia dysmorphism syndrome (733033001)
  • Spinocerebellar ataxia type 1 (715748006)
  • Spinocerebellar ataxia type 10 (715754007)
  • Spinocerebellar ataxia type 11 (719207000)
  • Spinocerebellar ataxia type 12 (719208005)
  • Spinocerebellar ataxia type 13 (719209002)
  • Spinocerebellar ataxia type 14 (719210007)
  • Spinocerebellar ataxia type 15/16 (716724006)
  • Spinocerebellar ataxia type 17 (719249005)
  • Spinocerebellar ataxia type 18 (719250005)
  • Spinocerebellar ataxia type 19 (719251009)
  • Spinocerebellar ataxia type 2 (715751004)
  • Spinocerebellar ataxia type 20 (718771009)
  • Spinocerebellar ataxia type 21 (718774001)
  • Spinocerebellar ataxia type 23 (718772002)
  • Spinocerebellar ataxia type 25 (718770005)
  • Spinocerebellar ataxia type 26 (718769009)
  • Spinocerebellar ataxia type 27 (719252002)
  • Spinocerebellar ataxia type 28 (715824008)
  • Spinocerebellar ataxia type 29 (715825009)
  • Spinocerebellar ataxia type 30 (719253007)
  • Spinocerebellar ataxia type 31 (715826005)
  • Spinocerebellar ataxia type 32 (719254001)
  • Spinocerebellar ataxia type 34 (719255000)
  • Spinocerebellar ataxia type 35 (719300001)
  • Spinocerebellar ataxia type 36 (711158005)
  • Spinocerebellar ataxia type 37 (719301002)
  • Spinocerebellar ataxia type 38 (734021001)
  • Spinocerebellar ataxia type 4 (715755008)
  • Spinocerebellar ataxia type 40 (734020000)
  • Spinocerebellar ataxia type 5 (719302009)
  • Spinocerebellar ataxia type 6 (715752006)
  • Spinocerebellar ataxia type 7 (715726000)
  • Spinocerebellar ataxia type 8 (715753001)
  • Spinocerebellar ataxia with axonal neuropathy type 1 (765091006)
  • Spinocerebellar degeneration and corneal dystrophy syndrome (720750004)
  • Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (715465001)
  • Spinocerebellar disease (91502009)
  • Spinocerebellar disease NOS (192883005)
  • Spinocerebellar disease NOS (646141000000103)
  • Vestibulocerebellar ataxia (22443004)
  • X-linked sideroblastic anemia with spinocerebellar ataxia (719816006)
  • X-linked spinocerebellar ataxia type 3 (719817002)
  • X-linked spinocerebellar ataxia type 4 (719818007)