@prefix p: <http://www.wikidata.org/prop/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix schema1: <http://schema.org/> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix wd: <http://www.wikidata.org/entity/> .
@prefix wds: <http://www.wikidata.org/entity/statement/> .
@prefix wdt: <http://www.wikidata.org/prop/direct/> .
@prefix wdtn: <http://www.wikidata.org/prop/direct-normalized/> .
@prefix wikibase: <http://wikiba.se/ontology#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

wd:Q1707822 rdfs:label "متلازمة بيندريد"@ar,
        "Pendredov sindrom"@bs,
        "Pendredův syndrom"@cs,
        "Pendred-Syndrom"@de,
        "Pendred syndrome"@en,
        "Síndrome de Pendred"@es,
        "Pendredin oireyhtymä"@fi,
        "syndrome de Pendred"@fr,
        "Պենդրեդի համախտանիշ"@hy,
        "sindrome di Pendred"@it,
        "Пендред синдром"@mk,
        "Syndroom van Pendred"@nl,
        "Zespół Pendreda"@pl,
        "Síndrome Pendred"@pt,
        "Síndrome Pendred"@pt-br,
        "Синдром Пендреда"@ru,
        "Pendredov sindrom"@sl,
        "Pendred综合征"@zh,
        "Pendred综合征"@zh-hans ;
    schema1:dateModified "2026-10-24T00:31:46+00:00"^^xsd:dateTime ;
    schema1:description "مرض وراثي"@ar,
        "Krankheit"@de,
        "genetic disorder"@en,
        "Maladie génétique"@fr,
        "malattia genetica"@it,
        "genetska bolezen"@sl,
        "хвороба"@uk ;
    schema1:version 2560166594 ;
    wikibase:identifiers 20,
        22 ;
    wikibase:sitelinks 14 ;
    wikibase:statements 55 ;
    skos:altLabel "Dyshormogene Struma"@de,
        "Familiäre dyshormogene Struma"@de,
        "Hypothyroidism, Congenital, Due to Dyshormonogenesis, 2B"@en,
        "PDS"@en,
        "PENDRED SYNDROME; PDS"@en,
        "Pendred Syndrome"@en,
        "TDH2B"@en,
        "Thyroid Hormonogenesis, Genetic Defect In, 2B"@en,
        "congenital hypothyroidism due to dyshormonogenesis 2B"@en,
        "deafness with goiter"@en,
        "genetic defect in thyroid hormonogenesis 2B"@en,
        "goiter-deafness syndrome"@en,
        "thyroid dyshormonogenesis 2B"@en,
        "Sindrome de Pendred"@es,
        "Pendredin syndrooma"@fi,
        "dyshormonosynthèse thyroïdienne 2B"@fr,
        "Pendred syndroom"@nl,
        "rodbinska dishormogena golša"@sl ;
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    p:P1193 wds:Q1707822-D2F9FC7F-794B-4E09-8C48-25AD04AB485B ;
    p:P1417 wds:Q1707822-EE212331-98D1-47B8-AE50-EB49BAE48838 ;
    p:P14914 wds:Q1707822-CC537AA4-C121-4FA4-9195-10A574A6BC3F ;
    p:P1550 wds:Q1707822-0A0540A6-A09F-499B-A506-847CCADBFEDC ;
    p:P1748 wds:Q1707822-9DA3C5A6-7179-4AE4-AA66-F2AB26CB7777 ;
    p:P1995 wds:Q1707822-B74107C3-6C66-4A54-82F3-1C2A843504D1 ;
    p:P2293 wds:Q1707822-4C10B464-630A-4DFC-9A02-861BC8A5FD3F,
        wds:Q1707822-6750EDD3-276F-497D-8F25-F47FB63D224F,
        wds:Q1707822-A72C71A9-819E-4052-957C-5C3B2BC4507D ;
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        wds:Q1707822-5ACB69FC-4299-434A-85D9-5B64679B5A65,
        wds:Q1707822-68F1C85C-BCBE-4B71-88E7-42589561DB29,
        wds:Q1707822-7416a4d8-48bf-52d2-a084-60a6f6c080cb,
        wds:Q1707822-CBE61EC2-B0AD-45B6-9158-C111085F020B,
        wds:Q1707822-D4D9EA57-4A47-4F83-97EF-CAF7A24D2323,
        wds:Q1707822-D9AD5A06-13E6-4C4C-92A2-AF731C05A506,
        wds:Q1707822-F0395C22-31E0-486B-A25E-EB6D3517F38E ;
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        wds:Q1707822-FFE2219A-20EC-4B6C-A88E-09196BD979C8 ;
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        wds:Q1707822-D034F9B5-8414-4021-8C48-34FD2074C838 ;
    p:P4229 wds:Q1707822-CC842595-DA23-46C8-920E-C1BA8073D62D ;
    p:P4317 wds:Q1707822-9EC8C34D-2A90-4F42-A67F-0EDBB75DC8F4 ;
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    p:P5008 wds:Q1707822-2C15E2AD-2831-4983-8565-A0942AB98755 ;
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        wds:Q1707822-F8D5767A-CAAC-4F93-8970-ABFCC7E7B223 ;
    p:P646 wds:Q1707822-33513841-CE34-4A49-B78A-78145522D10C ;
    p:P6532 wds:Q1707822-1B4C3B3C-DE59-4B6B-B5D8-DAE80EA17149,
        wds:Q1707822-1DB66E46-1723-45CC-B7D2-7597BC4AD071,
        wds:Q1707822-21A70886-F8F9-4F02-B5BF-A3DC3FCC0FA7,
        wds:Q1707822-25A970EB-321D-4BBF-81C9-74A776DE4BF6,
        wds:Q1707822-48A575E1-B76A-4C3D-9710-E0FBAD4D9717,
        wds:Q1707822-59FAA876-79C8-4517-9A73-9F4A2A1F2A95,
        wds:Q1707822-61B9A4A1-7D8E-4A2C-BD82-5B40545C6037,
        wds:Q1707822-723B4091-8478-495E-AFF7-399548DA2D8F,
        wds:Q1707822-7AACA69C-26DE-4CCF-99CD-A46BC43408F6,
        wds:Q1707822-B3203213-BBA1-4A45-A3A5-349107C21CF0,
        wds:Q1707822-C5565090-2CA0-4A5A-9043-726ADF6C8F1A,
        wds:Q1707822-EE27BA49-0BC7-4B94-AC18-EBE144B1F7B2 ;
    p:P668 wds:q1707822-015D8AAB-182A-4686-8FC5-EC378E8B92E7 ;
    p:P699 wds:Q1707822-1E3817F3-6E7C-4E90-8CFE-8921FDF132FE ;
    p:P7329 wds:Q1707822-4F2A80F8-5EA9-464C-86E7-FA69C853BC8A ;
    p:P7464 wds:Q1707822-D6B436D1-D1B2-48B9-8117-70CC0CE897B1 ;
    p:P7807 wds:Q1707822-6646DF1D-7F0D-43C4-9BDD-728F9A23B338 ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/C536648> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0010134> ;
    wdtn:P5806 <http://snomed.info/id/70348004> ;
    wdtn:P6366 <https://makg.org/entity/2781419390>,
        <https://makg.org/entity/2910086011> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060744> ;
    wdt:P11143 "Pendred syndrome" ;
    wdt:P11430 "DI-00905" ;
    wdt:P1193 0.00005 ;
    wdt:P1417 "science/Pendreds-syndrome" ;
    wdt:P14914 "D00705" ;
    wdt:P1550 "705" ;
    wdt:P1748 "C121745" ;
    wdt:P1995 wd:Q162606 ;
    wdt:P2293 wd:Q14907462,
        wd:Q17928744,
        wd:Q18028187 ;
    wdt:P279 wd:Q10267817,
        wd:Q179630,
        wd:Q55785710,
        wd:Q55788734,
        wd:Q7799748 ;
    wdt:P2841 wd:Q21953125,
        wd:Q21955199 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0060744>,
        <http://purl.obolibrary.org/obo/DOID_0060744>,
        <http://www.orpha.net/ORDO/Orphanet_705> ;
    wdt:P2892 "C0271829" ;
    wdt:P31 wd:Q112193867,
        wd:Q929833 ;
    wdt:P4229 "E07.1" ;
    wdt:P4317 "4271" ;
    wdt:P486 "C536648" ;
    wdt:P492 "274600" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0010134" ;
    wdt:P557 "9771" ;
    wdt:P5806 "70348004" ;
    wdt:P6366 "2781419390",
        "2910086011" ;
    wdt:P646 "/m/04ykk4" ;
    wdt:P6532 wd:Q1054718,
        wd:Q10686316,
        wd:Q1282114,
        wd:Q1344835,
        wd:Q154709,
        wd:Q16501,
        wd:Q18556131,
        wd:Q2241556,
        wd:Q3317827,
        wd:Q4116448,
        wd:Q767485,
        wd:Q928697 ;
    wdt:P668 "NBK1467" ;
    wdt:P699 "DOID:0060744" ;
    wdt:P7329 "5A00.02" ;
    wdt:P7464 "pendred-syndrome" ;
    wdt:P7807 "1156056623" .