rdfs: label
"spinocerebellar ataxia type 15/16"@en
skos: altLabel
"SCA15"@en
"SCA15/16"@en
"SPINOCEREBELLAR ATAXIA 15"@en
"SPINOCEREBELLAR ATAXIA 15; SCA15"@en
"Spinocerebellar Ataxia 16"@en
"Spinocerebellar Ataxia 16, Formerly"@en
"Spinocerebellar Ataxia type 15"@en
"spinocerebellar ataxia type 16"@en
schema: description
ar
de
en
uk
"Krankheit"@de
"Spinocerebellar ataxia type 15/16 (SCA15/16) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by cerebellar ataxia, tremor and cognitive impairment."@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
schema: dateModified
"2026-07-05T12:52:49+00:00"^^xsd:dateTime
schema: version
2514126475
wikibase: identifiers
10
wikibase: sitelinks
0
wikibase: statements
21
p: P11430
wd: statement/Q21097863-5563148c-4a74-dd16-0693-afbc081f1cec
p: P1550
wd: statement/Q21097863-22DC068D-50B5-45CF-AB7F-48779ED56AD3
wd: statement/Q21097863-DC49C000-6D94-4B34-9167-0A8586C57F33
p: P2293
wd: statement/Q21097863-C3AA3CE4-A042-43D9-B0B5-3AD049442D68
p: P279
wd: statement/Q21097863-1E4FB718-688C-4DB3-A3F5-0D8980F3DB84
wd: statement/Q21097863-20EAB4B1-9B2A-428D-916E-F1952C4538BC
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wd: statement/Q21097863-A43E6600-65FC-42EC-880A-49485FDC8810
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wd: statement/Q21097863-E3FE6B21-3BE8-461C-8138-3827957AD412
p: P2892
wd: statement/Q21097863-378248F0-C3F8-41AE-8501-858430679D4D
wd: statement/Q21097863-B5B3C256-8529-4121-A6DE-FC7BB029E63A
p: P31
wd: statement/Q21097863-7220843E-402A-40EC-8019-2411A976DD8C
wd: statement/Q21097863-E340512A-5B52-49F9-8D8A-81A10B2B6A23
p: P4229
wd: statement/Q21097863-AF2D9A7C-6E2F-4618-A062-3162A4BD4B35
p: P4317
wd: statement/Q21097863-878554DB-94D9-468F-A086-4AECEA93D4DD
p: P492
wd: statement/Q21097863-4BCE9189-182F-457F-925E-D842AE6111D6
p: P5008
wd: statement/Q21097863-0ACD0745-C9D3-41A5-820B-7BD2EE00AC5E
p: P5270
wd: statement/Q21097863-542E79BA-CE2C-4A20-A775-346C8FA6B8C8
p: P699
wd: statement/Q21097863-D6C75499-EB0B-48CD-8145-772152622014
p: direct-normalized/P5270
<http://purl.obolibrary.org/obo/MONDO_0011694>
p: direct-normalized/P699
<http://purl.obolibrary.org/obo/DOID_DOID:0050965>
wdt: P11430
"DI-01078"
wdt: P1550
"98769"
"98770"
wdt: P2293
ITPR1
wdt: P279
autosomal dominant cerebellar ataxia type I
wdt: P2888
<http://identifiers.org/doid/DOID:0050965>
<http://purl.obolibrary.org/obo/DOID_0050965>
<http://www.orpha.net/ORDO/Orphanet_98769>
<http://www.orpha.net/ORDO/Orphanet_98770>
wdt: P2892
"C1847725"
"C2676005"
wdt: P31
type of disease
rare disease
wdt: P4229
"G11.2"
wdt: P4317
"10477"
wdt: P492
"606658"
wdt: P5008
WikiProject Medicine
wdt: P5270
"MONDO_0011694"
wdt: P699
"DOID:0050965"