dystonia 12

human disease
rdfs:label
"dystonia 12"@en
skos:altLabel "DYSTONIA 12; DYT12"@en
"DYT-ATP1A3"@en
"DYT12"@en
"Dystonia 12"@en
"Dystonia type 12"@en
"Dystonia-Parkinsonism, Rapid-Onset"@en
"Rapid-onset dystonia-parkinsonism"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-24T00:32:33+00:00"^^xsd:dateTime
schema:version 2560166712
wikibase:identifiers 11
9
wikibase:sitelinks 0
wikibase:statements 42
p:P11430 wd:statement/Q32038818-c0236d9e-4926-225f-a296-ec161ae06979
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p:P1550 wd:statement/Q32038818-58947B3A-6B24-4837-A7B7-711DDB9F1583
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p:P1995 wd:statement/Q32038818-BF1B502F-2FF6-46CA-8C11-FC99BA4066EE
p:P2293 wd:statement/Q32038818-ED438E0A-A606-4557-9B0D-4664648AA2D9
p:P279 wd:statement/Q32038818-13BEFF26-E0E7-4CA0-9FF1-86391724DE49
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wd:statement/Q32038818-99B2F171-D2D5-4445-9EE7-A15520515EC1
wd:statement/Q32038818-BC540B55-20D5-466D-8E1A-496AD325A7A6
p:P2888 wd:statement/Q32038818-0E2487FF-A221-4597-A922-974636BA423E
wd:statement/Q32038818-86259A7E-2562-41F0-97E3-D78045DF7025
p:P2892 wd:statement/Q32038818-A5566EB4-0D9D-4E0C-BAF7-52DEF40E1C57
p:P31 wd:statement/Q32038818-51E3FBC1-E1B3-4390-A18B-1463D5000611
wd:statement/Q32038818-AE9BE2E9-A564-47C1-A918-6FEE87498E3E
p:P4229 wd:statement/Q32038818-3687A6C4-45BB-40CE-B70A-00DAD8DBF12B
p:P4317 wd:statement/Q32038818-E05EA2E1-44E6-416C-8AEA-84C23C66A3AB
p:P492 wd:statement/Q32038818-E849FC60-A2AD-486B-9E58-03556FF31527
p:P5008 wd:statement/Q32038818-60076E19-2BE4-4BCE-8DBB-5242F7E0FEA9
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p:P6532 wd:statement/Q32038818-10131BAD-5B7D-48BC-B372-76F84E5088EC
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wd:statement/Q32038818-5D09314A-312A-49F2-9745-201618E862DB
wd:statement/Q32038818-6C485C4C-69B2-4B63-9F62-DB1A8C22BFEE
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wd:statement/Q32038818-944EFD8E-35F5-49B7-8B1E-E42A72ABD3C0
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wd:statement/Q32038818-D47BD2AE-4F6E-4AD1-9FDE-9467A64206C7
p:P699 wd:statement/Q32038818-65308296-AE4E-4CB4-B211-A7660A3562D5
p:P7464 wd:statement/Q32038818-F491508E-70DB-4B31-A70D-C6A00389A921
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0007496>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0090056>
wdt:P11430 "DI-00419"
wdt:P1193 0.000001^^xsd:decimal
wdt:P14914 "D71517"
wdt:P1550 "71517"
wdt:P1748 "C157577"
wdt:P1995 neurology
wdt:P2293 ATP1A3
wdt:P279 autosomal dominant disease
rare genetic parkinsonian disorder
persistent combined dystonia
dystonia
wdt:P2841 childhood onset
juvenile onset
adult onset
wdt:P2888 <http://identifiers.org/doid/DOID:0090056>
<http://purl.obolibrary.org/obo/DOID_0090056>
wdt:P2892 "C1868681"
wdt:P31 type of disease
rare disease
wdt:P4229 "G24.1"
wdt:P4317 "9628"
wdt:P492 "128235"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0007496"
wdt:P6532 hypokinesia
motor delay
Generalized hypotonia
parkinsonian syndrome
anxiety
ataxia
childhood onset
dysarthria
cerebellar atrophy
congenital torticollis
depression
dysphagia
seizure
muteness
hypersalivation
wdt:P699 "DOID:0090056"
wdt:P7464 "rapid-onset-dystonia-parkinsonism"
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