SHMARQL

corticobasal degeneration

<http://www.wikidata.org/entity/Q1755684>

progressive neurodegenerative condition affecting the cerebral cortex and basal ganglia
rdfs:label
"corticobasal degeneration"@en
skos:altLabel
"CBGD"@en
"Cortical Basal Ganglionic Degeneration"@en
"Cortical-Basal Ganglionic degeneration"@en
"Cortico-Basal Ganglionic Degeneration (CBGD)"@en
"Corticobasal Degeneration"@en
"Corticobasal syndrome"@en
"cortical basal ganglionic degeneration"@en
"corticobasal degeneration disorder"@en
"corticodentatonigral degeneration with neuronal achromasia"@en
schema:description
"progressive neurodegenerative condition affecting the cerebral cortex and basal ganglia"@en
schema:dateModified "2026-10-24T00:20:44+00:00"^^xsd:dateTime
schema:version 2560164945
wikibase:identifiers 20
22
wikibase:sitelinks 18
wikibase:statements 51
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p:P1550 wd:statement/Q1755684-25C93AE2-7CE2-4288-AAD8-B327C7733924
p:P1748 wd:statement/Q1755684-5841DFAE-3AE0-46E5-8F1B-F5EC38DEABA2
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wd:statement/Q1755684-73174D9E-6FE3-4484-B896-DF38F345A6DA
p:P2888 wd:statement/Q1755684-73756C29-946F-4E48-A789-FF06A7FFB07B
p:P2892 wd:statement/Q1755684-36DF9C25-DCEF-4222-8693-A17E1446951E
p:P31 wd:statement/Q1755684-01b9d599-4f1a-ade4-d280-f7df13e04220
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p:P5270 wd:statement/Q1755684-8BA38562-901B-46EF-AA0D-B3973423F288
p:P557 wd:statement/q1755684-4C991C80-22C2-4B0C-AD6B-D31D917098C4
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wd:statement/Q1755684-B5463670-8124-48AD-A1CC-AA9C007ED4F3
wd:statement/Q1755684-C0F89E8F-B10F-49E6-9D59-875E4A07EC05
wd:statement/Q1755684-C774FA13-D10E-45A4-BE5C-21C7551AAD8F
wd:statement/Q1755684-DA58F977-BAE6-46F8-98FB-92649385CE0F
wd:statement/Q1755684-E2FA5C68-939D-443E-9F4B-47BC70C8828C
wd:statement/Q1755684-EAD94ED3-412C-48D8-8D2F-B88E18202C99
p:P672 wd:statement/Q1755684-543de30c-4ad0-14c1-ef11-277288382a71
p:P673 wd:statement/q1755684-E7971F70-20BC-478C-8F9E-8ADED7A7E2A4
p:P7329 wd:statement/Q1755684-b19e185c-4933-3ecc-3fe1-64b607e081ba
p:P7807 wd:statement/Q1755684-562136f1-49c9-f9b3-a172-39ff59e00a6b
p:P7995 wd:statement/Q1755684-4BCC7DD5-A5A1-4AA5-B7AA-4CA9AB9C63C5
p:direct-normalized/P4527 <http://data.parliament.uk/terms/481508>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D000088282>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0022880>
p:direct-normalized/P5806 <http://snomed.info/id/18842008>
p:direct-normalized/P6366 <https://makg.org/entity/2776936178>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C10.574.945.312>
wdt:P10283 "C2776936178"
wdt:P11143 "Corticobasal degeneration"
wdt:P1325 <http://www.nanbyou.or.jp/entry/142>
wdt:P14914 "D454887"
wdt:P1550 "454887"
wdt:P1748 "C129069"
wdt:P1813 "CBD"@en
wdt:P279 cerebral degeneration
frontotemporal dementia
wdt:P2841 adult onset
late onset
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_454887>
wdt:P2892 "C0393570"
wdt:P31 type of disease
designated intractable/rare disease
rare disease
wdt:P3417 "Corticobasal-Degeneration"
wdt:P373 "Corticobasal degeneration"
wdt:P4233 "corticobasal-degeneration"
wdt:P4317 "46"
wdt:P4527 "481508"
wdt:P486 "D000088282"
wdt:P493 "331.6"
wdt:P5270 "MONDO_0022880"
wdt:P557 "33284"
wdt:P5806 "18842008"
wdt:P6366 "2776936178"
wdt:P646 "/m/086d8q"
wdt:P6532 hypokinesia
involuntary movement
myoclonus
Oromotor apraxia
Limb apraxia
Limb myoclonus
parkinsonian syndrome
hypoesthesia
tremor
movement disorders
aphasia
behavioral abnormality
memory disorder
akinesia
Frontal release sign
gait abnormality
dementia
dystonia
wdt:P672 "C10.574.945.312"
wdt:P673 "1150039"
wdt:P7329 "8A00.1Y"
wdt:P7807 "598493320"
wdt:P7995 "corticobasal-degeneration"
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