SHMARQL

semantic dementia

<http://www.wikidata.org/entity/Q18587>

progressive neurodegenerative disorder
rdfs:label
"semantic dementia"@en
skos:altLabel
"Dementia, Frontotemporal, With Parkinsonism"@en
"Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex"@en
"FRONTOTEMPORAL DEMENTIA"@en
"FRONTOTEMPORAL DEMENTIA; FTD"@en
"FTD"@en
"Frontotemporal Dementia With Parkinsonism"@en
"Frontotemporal Lobar Degeneration With Tau Inclusions"@en
"Frontotemporal Lobe Dementia"@en
"Ftdp17"@en
"Ftld With Tau Inclusions"@en
"Multiple System Tauopathy With Presenile Dementia"@en
"Pallidopontonigral Degeneration"@en
"Pick Complex"@en
"Semantic primary progressive aphasia"@en
"Semantic variant PPA"@en
"Wilhelmsen-Lynch Disease"@en
schema:description
"progressive neurodegenerative disorder"@en
schema:dateModified "2026-10-23T23:17:23+00:00"^^xsd:dateTime
schema:version 2560151920
wikibase:identifiers 16
wikibase:sitelinks 7
wikibase:statements 43
p:P10283 wd:statement/Q18587-5FB25904-92D1-4672-8005-BC7309764E3C
p:P1193 wd:statement/Q18587-A55BD3E6-6A9F-482A-8029-55EB9C41FFBB
p:P14914 wd:statement/Q18587-5A96B7D9-F872-450C-ADBA-CBFEC5BB47BE
p:P1550 wd:statement/Q18587-E8D70059-7C19-44EB-A682-7DA52A878806
p:P1995 wd:statement/Q18587-c0f9ed43-4a41-0a9f-ce08-6c782e550d7b
p:P2293 wd:statement/Q18587-04F2D35B-4E0D-41D6-8F95-D0670FB7A141
wd:statement/Q18587-80E3093F-1C26-4C4A-8FAC-8D656C1F31B0
wd:statement/Q18587-A10AB745-33F1-477C-8531-3E16963466AF
wd:statement/Q18587-A91ACFF1-687D-466E-A38C-8668A90C44D4
wd:statement/Q18587-B6759AE5-8570-4BB9-8EEB-A994CB472AB5
wd:statement/Q18587-C46BE0AF-D577-4FEB-AAB8-533C30FD6EA5
wd:statement/Q18587-ED78F25E-C1B8-48F7-A3F1-C88623EA6353
p:P279 wd:statement/Q18587-0B7221E3-8E8D-40C8-A0D2-FBBC9976B909
wd:statement/Q18587-AA064870-C2CA-4C72-AA1F-4A0EBAB0FF8B
p:P2841 wd:statement/Q18587-4CEB67D5-EA77-4E9A-A657-C4D04678C316
p:P2888 wd:statement/Q18587-ADFD684C-4364-49F2-8AD9-63BD66FE7FC3
p:P2892 wd:statement/Q18587-458BA99C-CD95-43F3-9376-CC38D89FD7A8
wd:statement/Q18587-D5200C55-BB98-477C-B2F0-074705308A61
wd:statement/Q18587-E98699DF-9D20-4CAC-AE15-886CE503A144
wd:statement/Q18587-FF72A57E-A055-4554-9C88-01798C96656A
p:P31 wd:statement/Q18587-440356CC-F20D-4113-B861-56092D9A4C76
p:P3841 wd:statement/Q18587-EB1A1D70-6985-48DD-9F24-D82B349ABEA2
p:P4229 wd:statement/Q18587-E0244D63-51D3-4A52-96FE-2AE686EEA848
p:P4317 wd:statement/Q18587-87E741F0-AF46-4626-9DA6-390E594DC706
p:P492 wd:statement/Q18587-BBD3A328-C16C-4C6F-90A3-1F044471D6F0
p:P493 wd:statement/Q18587-E342877F-1B98-4F2E-81F9-CCDD58B1541F
p:P5270 wd:statement/Q18587-9F783CEB-5BFF-417E-A8B8-80C13D311797
p:P6366 wd:statement/Q18587-49293A10-4037-4B96-9852-F10127696ADD
p:P646 wd:statement/Q18587-2B0D9E38-5E55-40F0-866D-2E4BEC7DB905
p:P6532 wd:statement/Q18587-108E0718-0517-402C-A7C6-42EE2E3CC136
wd:statement/Q18587-36578500-73D7-4241-9F23-DEEC596DA683
wd:statement/Q18587-3DB8BBDB-5758-4EBB-86BA-66EB311E6FF6
wd:statement/Q18587-85ED6C6F-704E-43F9-B581-203BC44BEDCD
wd:statement/Q18587-92362F6F-0C03-43A8-8C23-C9398D8AAAA1
wd:statement/Q18587-9A784D62-F297-457D-9FCF-C5B49A1F0E0A
wd:statement/Q18587-A5D21D14-08B7-49A4-8725-D3D562E5C4F4
wd:statement/Q18587-A95D80A5-667A-4D89-BE1A-710C2948C9BA
wd:statement/Q18587-B7348025-10FA-4382-98FB-B928C0D217F7
wd:statement/Q18587-C69265D0-6D10-4FD7-A9E6-E5EF94EECCE1
wd:statement/Q18587-C9D9E77F-0E3A-4730-8C77-D1013AF97E9F
wd:statement/Q18587-E272280A-3EF0-4772-BAC3-BF854F2EF056
wd:statement/Q18587-F044BA5D-D6A0-48B1-8608-7D36AB1972DB
p:P668 wd:statement/Q18587-dbfccd33-4cf8-13c3-30ef-ab759886ede7
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0010857>
p:direct-normalized/P6366 <https://makg.org/entity/2779116556>
wdt:P10283 "C2779116556"
wdt:P1193 0.000001^^xsd:decimal
wdt:P14914 "D100069"
wdt:P1550 "100069"
wdt:P1995 neurology
wdt:P2293 MAPT
GRN
CHMP2B
TREM2
TMEM106B
PSEN1
C9orf72
wdt:P279 progressive nonfluent aphasia
behavioral variant of frontotemporal dementia
wdt:P2841 adult onset
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_100069>
wdt:P2892 "C0338451"
"C0338462"
"C1838313"
"C1862937"
wdt:P31 type of disease
wdt:P3841 "HP:0030219"
wdt:P4229 "G31.0"
wdt:P4317 "10792"
wdt:P492 "600274"
wdt:P493 "331.19"
wdt:P5270 "MONDO_0010857"
wdt:P6366 "2779116556"
wdt:P646 "/m/06xs_3"
wdt:P6532 visual verbal agnosia
speech disorder
dyslexia
Middle age onset
parkinsonian syndrome
visual agnosia
amyotrophic lateral sclerosis
aphasia
brain atrophy
aboulia
anomic aphasia
dysgraphia
dementia
wdt:P668 "NBK1505"
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data from SPARQL profile: Wikidata