rdfs: label
en
pt
pt-br
"Ataxia espinocerebelosa tipo 37"@pt
"Ataxia espinocerebelosa tipo 37"@pt-br
"spinocerebellar ataxia type 37"@en
skos: altLabel
"SCA37"@en
"SPINOCEREBELLAR ATAXIA 37"@en
"SPINOCEREBELLAR ATAXIA 37; SCA37"@en
"Spinocerebellar ataxia with altered vertical eye movements"@en
schema: description
ar
de
en
uk
"Krankheit"@de
"Spinocerebellar ataxia type 37 (SCA37) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1; see this term), characterized by a cerebellar syndrome along with altered vertical eye movements"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
schema: dateModified
"2026-10-24T00:12:16+00:00"^^xsd:dateTime
schema: version
2560163463
wikibase: identifiers
9
wikibase: sitelinks
0
wikibase: statements
36
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p: P2841
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p: P2888
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p: direct-normalized/P5270
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wdt: P11430
"DI-05050"
wdt: P1193
0.000001^^xsd:decimal
wdt: P14914
"D363710"
wdt: P1550
"363710"
wdt: P2293
DAB1
SCA37
wdt: P279
autosomal dominant cerebellar ataxia type I
wdt: P2841
adult onset
wdt: P2888
<http://identifiers.org/doid/DOID:0050984>
<http://purl.obolibrary.org/obo/DOID_0050984>
<http://www.orpha.net/ORDO/Orphanet_363710>
wdt: P2892
"C3889636"
wdt: P31
type of disease
wdt: P4229
"G11.8"
wdt: P4317
"12368"
wdt: P492
"615945"
wdt: P5008
WikiProject Medicine
wdt: P5270
"MONDO_0014410"
wdt: P6532
Abnormal conjugate eye movement
myoclonus
dysdiadochokinesia
speech disorder
Falls
Cerebellar vermis atrophy
Diffuse cerebellar atrophy
cogwheel rigidity
hypoesthesia
pathologic nystagmus
tremor
dysphagia
truncal ataxia
gait abnormality
sensorineural hearing loss
wdt: P699
"DOID:0050984"