|
rdfs:label
|
"autosomal recessive juvenile Parkinson disease 2"@en
|
|
skos:altLabel
|
"PARK2"@en
|
|
"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"@en
|
|
"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2"@en
|
|
"Parkinson Disease, Juvenile, Autosomal Recessive"@en
|
|
"Parkinsonism, Early-Onset, With Diurnal Fluctuation"@en
|
|
"autosomal recessive juvenile Parkinson disease type 2"@en
|
|
"autosomal recessive juvenile Parkinson's disease 2"@en
|
|
schema:description
|
"Krankheit"@de
"Parkinson's disease that has material basis in mutation in the parkin gene (PARK2) on chromosome 6q25.2-q27"@en
"хвороба"@uk
|
|
schema:dateModified
|
"2026-07-05T12:33:38+00:00"^^xsd:dateTime
|
|
schema:version
|
2514121521
|
|
wikibase:identifiers
|
5
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
16
|
|
p:P11430
|
wd:statement/Q21154041-f2a8f0ef-42ad-2782-db01-1cdf92b6eae1
|
|
p:P1748
|
wd:statement/Q21154041-b52e6091-42b9-eedd-eb00-2ca70cd9cbeb
|
|
p:P2293
|
wd:statement/Q21154041-6248E622-3E5E-4E30-BF07-347EA372E8B3
|
|
p:P279
|
wd:statement/Q21154041-501FB485-C871-4152-9B30-51A6D6F3D5D1
|
|
wd:statement/Q21154041-59399F79-659E-4F56-B98E-3D460AD21732
|
|
wd:statement/Q21154041-A9835C17-AE0C-4BA9-92DE-5CD0D26FC168
|
|
p:P2888
|
wd:statement/Q21154041-97C693DD-A07E-4142-927B-7C00358A4D4E
|
|
wd:statement/Q21154041-A5778A1D-53F5-470A-9FA8-445AEFE0D7A6
|
|
wd:statement/Q21154041-E12D1354-6B8F-4612-9256-9B6AA17E4F36
|
|
p:P2892
|
wd:statement/Q21154041-BCC9EDE6-2497-48FF-9CB9-22A548F6D504
|
|
p:P31
|
wd:statement/Q21154041-3C2B253E-2589-45A5-8E65-C0E9BEF59254
|
|
wd:statement/Q21154041-AEBF0D1A-35BD-4BE8-8894-B4CF8C415702
|
|
p:P492
|
wd:statement/Q21154041-6847D2D5-F370-45F5-8331-9A060D85B21C
|
|
p:P5008
|
wd:statement/Q21154041-3E4B0B5E-9ECB-4456-B8D9-BF7BA375569F
|
|
p:P5270
|
wd:statement/Q21154041-DC19AD03-E2C5-4064-8384-1B2FCF706787
|
|
p:P699
|
wd:statement/Q21154041-08CF2812-5E12-42FE-BA0C-1DF08E06543C
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0010820>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0060368>
|
|
wdt:P11430
|
"DI-01238"
|
|
wdt:P1748
|
"C198603"
|
|
wdt:P2293
|
PRKN
|
|
wdt:P279
|
autosomal recessive disease
|
|
juvenile-onset Parkinson disease
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0060368>
|
|
<http://purl.obolibrary.org/obo/DOID_0060368>
|
|
<http://www.orpha.net/ORDO/Orphanet_2828>
|
|
wdt:P2892
|
"C1868675"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P492
|
"600116"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0010820"
|
|
wdt:P699
|
"DOID:0060368"
|