@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:Q2823332 rdfs:label "متلازمة كوستيف"@ar,
        "Costeff-Syndrom"@de,
        "3-methylglutaconic aciduria type 3"@en,
        "síndrome de Costeff"@es,
        "acidurie 3-méthylglutaconique type 3"@fr,
        "תסמונת קוסטף"@he,
        "sindrome di Costeff"@it,
        "zespół Costeffa"@pl,
        "Acidúria 3-metilglutacônica tipo 3"@pt,
        "Acidúria 3-metilglutacônica tipo 3"@pt-br,
        "sìndrome de Costeff"@vec ;
    schema1:dateModified "2026-10-24T00:30:22+00:00"^^xsd:dateTime ;
    schema1:description "مرض يصيب الإنسان"@ar,
        "Krankheit"@de,
        "3-methylglutaconic aciduria that has material basis in mutation in the OPA3 gene"@en,
        "aciduria orgánica caracterizada por la asociación de atrofia óptica y coreoatetosis con aciduria 3-metilglutacónica"@es,
        "maladie"@fr,
        "malattia"@it,
        "хвороба"@uk ;
    schema1:version 2560166394 ;
    wikibase:identifiers 15 ;
    wikibase:sitelinks 7 ;
    wikibase:statements 38 ;
    skos:altLabel "3-METHYLGLUTACONIC ACIDURIA, TYPE III"@en,
        "3-METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3"@en,
        "3-methylglutaconic aciduria type III"@en,
        "Costeff optic atrophy syndrome"@en,
        "Costeff syndrome"@en,
        "Iraqi-Jewish 'Optic Atrophy Plus'"@en,
        "Iraqi-Jewish optic atrophy plus"@en,
        "MGA3"@en,
        "MGCA3"@en,
        "Mga, Type 3"@en,
        "Opa3, Autosomal Recessive"@en,
        "Optic Atrophy 3, Autosomal Recessive"@en,
        "Optic Atrophy Plus Syndrome"@en,
        "Optic Atrophy, Infantile, With Chorea and Spastic Paraplegia"@en,
        "autosomal recessive optic atrophy plus syndrome"@en,
        "autosomal recessive optic atrophy type 3"@en,
        "infantile optic atrophy with chorea and spastic paraplegia"@en,
        "Acidurie 3-methylglutaconique type 3"@fr,
        "Acidurie 3-méthylglutaconique Type 3"@fr,
        "atrophie optique de Costeff"@fr,
        "3-metilglutaril aciduria di tipo III"@it,
        "atrofia ottica di Costeff"@it,
        "sindrome da atrofia ottica di Costeff"@it,
        "acyduria 3-metyloglutakonowa typu 3"@pl,
        "acyduria 3-metyloglutakonowa typu III"@pl,
        "kwasica 3-metyloglutakonowa typu III"@pl ;
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    p:P138 wds:Q2823332-11ecf758-4644-603d-1078-46a078129093 ;
    p:P14914 wds:Q2823332-5B2B2E9E-4D09-4653-B6E9-1A095BE2E90A ;
    p:P1550 wds:Q2823332-9e3f3acf-4c96-94d1-2562-4d76f5aafd01 ;
    p:P2293 wds:Q2823332-4A13F031-2D9C-4ABE-9F79-F9681D321A1C,
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        wds:Q2823332-43B704C6-DECF-47F6-AE23-C2FA0814B7F7,
        wds:Q2823332-44663A1A-02C0-4608-A97D-90C4A20BC4F8,
        wds:Q2823332-9feea57f-466f-3219-47be-8ff1a9df65d1 ;
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        wds:Q2823332-BE3B2371-D73D-4E37-86A5-DD8BAE6FEB25 ;
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        wds:Q2823332-724017FC-C400-4A9A-B661-0C300943CBB3 ;
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    p:P61 wds:Q2823332-6426b66d-484b-d015-c7fd-b0899be91b92 ;
    p:P6532 wds:Q2823332-0B3F2F57-ED62-4B9B-82BC-8606339A77EE,
        wds:Q2823332-451F5BFD-176F-4FD0-90C3-38DDF43DC184,
        wds:Q2823332-53BDFABE-ECBC-49EB-9EB3-AF780F04945E,
        wds:Q2823332-7A5AAF92-2CAF-43F2-8AEE-046B832038E4,
        wds:Q2823332-977A5990-54CA-424A-A1C1-6F4C1B4735A3,
        wds:Q2823332-B280C147-0CFC-4C58-9582-C50E5E8FB66C,
        wds:Q2823332-C7DADC37-4AD0-4905-AC5A-B1061FC296AE,
        wds:Q2823332-FEFA573F-3E08-4151-B474-3933BAAEAC3B ;
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    p:P699 wds:Q2823332-7386426C-B9A0-440C-8D11-A2AF965617BB ;
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    p:P7807 wds:Q2823332-9f0e8fd6-4136-1877-3cdd-4b8f78bbcd1f ;
    wdtn:P2671 <http://g.co/kg/g/122z2q4d> ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/C535311> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0009787> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0110004> ;
    wdt:P11430 "DI-00006" ;
    wdt:P138 wd:Q22958861 ;
    wdt:P14914 "D67047" ;
    wdt:P1550 "67047" ;
    wdt:P2293 wd:Q18046643,
        wd:Q18049644 ;
    wdt:P2671 "/g/122z2q4d" ;
    wdt:P279 wd:Q10267817,
        wd:Q3598794,
        wd:Q55345670,
        wd:Q55788215 ;
    wdt:P2841 wd:Q21955201 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0110004>,
        <http://purl.obolibrary.org/obo/DOID_0110004> ;
    wdt:P2892 "C0574084" ;
    wdt:P31 wd:Q112193867,
        wd:Q929833 ;
    wdt:P4229 "E71.1",
        "E71.111" ;
    wdt:P4317 "5663" ;
    wdt:P486 "C535311" ;
    wdt:P492 "258501" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0009787" ;
    wdt:P61 wd:Q22958861 ;
    wdt:P6532 wd:Q154709,
        wd:Q18558185,
        wd:Q225957,
        wd:Q3317827,
        wd:Q3693493,
        wd:Q55083510,
        wd:Q737460,
        wd:Q827017 ;
    wdt:P668 "NBK1473" ;
    wdt:P699 "DOID:0110004" ;
    wdt:P7464 "costeff-syndrome" ;
    wdt:P7807 "535412248" .