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rdfs:label
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"Hội chứng Zellweger"@vi
"Zellweger sendromu"@tr
"Zellweger sindromi"@uz
"Zellweger syndrome"@en
"Zellweger syndrome"@nl
"Zellweger-Syndrom"@de
"Zellweger-en sindrome"@eu
"Zellwegerin oireyhtymä"@fi
"Zellwegerjev sindrom"@sl
"Zellwegerov sindrom"@bs
"Zellwegers syndrom"@nb
"Zellwegers syndrom"@sv
"Zellwegerův syndrom"@cs
"Zespół Zellwegera"@pl
"sindrome di Zellweger"@it
"sindromo de Zellweger"@eo
"syndrome de Zellweger"@fr
"síndrome de Zellweger"@ca
"síndrome de Zellweger"@es
"síndrome de Zellweger"@pt
"Σύνδρομο Ζέλβεγκερ"@el
"תסמונת זלווגר"@he
"سندروم زلوگر"@fa
"متلازمة زيلويغر"@ar
"ცელვეგერის სინდრომი"@ka
"젤웨거 증후군"@ko
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skos:altLabel
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"Sindrome de Zellweger"@es
"ZS"@en
"cerebrohepatorenal syndrome"@en
"cerebrohepatorenalni sindrom"@sl
"congenital iron overload"@en
"peroxisome biogenesis disorder"@en
"síndrome cerebrohepatorenal"@ca
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schema:description
|
"Krankheit"@de
"congenital disorder of nervous system"@en
"malaltia metabòlica hereditària"@ca
"rara malattia congenita autosomica recessiva. Fa parte dei disturbi dei perossisomi"@it
"vrozená vada nervové soustavy"@cs
"хвороба"@uk
"اضطراب خلقي نادر"@ar
"بیماری"@fa
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schema:dateModified
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"2026-10-24T00:42:33+00:00"^^xsd:dateTime
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schema:version
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2560168184
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wikibase:identifiers
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35
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37
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wikibase:sitelinks
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21
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wikibase:statements
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68
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p:direct-normalized/P486
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p:direct-normalized/P5270
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<http://purl.obolibrary.org/obo/MONDO_0019609>
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p:direct-normalized/P6366
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<https://makg.org/entity/2777485865>
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p:direct-normalized/P665
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<http://www.kegg.jp/entry/H01342>
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p:direct-normalized/P672
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<http://id.nlm.nih.gov/mesh/C06.552.970>
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<http://id.nlm.nih.gov/mesh/C10.228.140.163.100.968>
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|
<http://id.nlm.nih.gov/mesh/C12.050.351.968.419.978>
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|
<http://id.nlm.nih.gov/mesh/C12.200.777.419.978>
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|
<http://id.nlm.nih.gov/mesh/C12.950.419.978>
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<http://id.nlm.nih.gov/mesh/C16.131.077.970>
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|
<http://id.nlm.nih.gov/mesh/C16.320.565.189.968>
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|
<http://id.nlm.nih.gov/mesh/C16.320.565.663.970>
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|
<http://id.nlm.nih.gov/mesh/C18.452.132.100.968>
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|
<http://id.nlm.nih.gov/mesh/C18.452.648.189.968>
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|
<http://id.nlm.nih.gov/mesh/C18.452.648.663.970>
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p:direct-normalized/P699
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<http://purl.obolibrary.org/obo/DOID_DOID:905>
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wdt:P10283
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"C2777485865"
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|
wdt:P10376
|
"medicine-and-dentistry/zellweger-syndrome"
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|
wdt:P1325
|
<http://www.nanbyou.or.jp/entry/4621>
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|
wdt:P138
|
Hans Zellweger
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wdt:P1417
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"science/Zellweger-syndrome"
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|
wdt:P14914
|
"D00912"
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|
wdt:P1550
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"912"
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|
wdt:P1748
|
"C85239"
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|
wdt:P1995
|
medical genetics
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wdt:P2293
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PEX1
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PEX6
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|
PEX7
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PEX10
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PEX12
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PEX13
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PEX14
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PEX19
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PEX2
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PEX3
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PEX11B
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PEX16
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PEX26
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PEX5
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wdt:P279
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eye degenerative disease
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Zellweger spectrum disorder
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peroxisomal biogenesis disorder
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wdt:P2841
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neonatal onset
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wdt:P2888
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<http://identifiers.org/doid/DOID:905>
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|
<http://purl.obolibrary.org/obo/DOID_905>
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|
<http://www.orpha.net/ORDO/Orphanet_912>
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|
wdt:P2892
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"C0043459"
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|
"C0751594"
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|
wdt:P31
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type of disease
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|
symptom or sign
|
|
designated intractable/rare disease
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rare disease
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wdt:P3471
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"53661"
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wdt:P3827
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"zellweger-syndrome"
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wdt:P4229
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"E71.510"
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|
"Q87.8"
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|
wdt:P4317
|
"7917"
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|
wdt:P4342
|
"Zellwegers_syndromspektrum"
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|
wdt:P486
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"D015211"
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|
wdt:P492
|
"617370"
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|
wdt:P493
|
"277.86"
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|
"759.8"
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|
wdt:P5008
|
WikiProject Medicine
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|
wdt:P5270
|
"MONDO_0019609"
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|
wdt:P557
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"14248"
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wdt:P6366
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"2777485865"
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|
wdt:P646
|
"/m/04fvmy"
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|
wdt:P6532
|
reduced tendon reflexes
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|
wdt:P665
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"H01342"
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|
wdt:P667
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"A90"
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|
wdt:P668
|
"NBK1448"
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|
wdt:P672
|
"C06.552.970"
|
|
"C10.228.140.163.100.968"
|
|
"C12.050.351.968.419.978"
|
|
"C12.200.777.419.978"
|
|
"C12.950.419.978"
|
|
"C16.131.077.970"
|
|
"C16.320.565.189.968"
|
|
"C16.320.565.663.970"
|
|
"C18.452.132.100.968"
|
|
"C18.452.648.189.968"
|
|
"C18.452.648.663.970"
|
|
wdt:P699
|
"DOID:905"
|
|
wdt:P7807
|
"226023718"
|