@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:Q3508565 rdfs:label "متلازمة إيه بي سي دي"@ar,
        "کۆنیشانەی ئەی-بی-سی-دی"@ckb,
        "ABCD syndrome"@en,
        "Síndrome ABCD"@es,
        "Syndrome ABCD"@fr,
        "Sindrome ABCD"@it,
        "Síndrome ABCD"@pt,
        "Síndrome ABCD"@pt-br,
        "АБЦД синдром"@sr,
        "ABCD sendromu"@tr,
        "sìndrome aBCD"@vec ;
    schema1:dateModified "2026-10-24T00:42:58+00:00"^^xsd:dateTime ;
    schema1:description "اضطراب صبغي جسدي متنحي، يتميز بحدوث برص ومنظرُ أسود للشعر واضطراب هجرة الخلايا في عصبونات الأمعاء، والصمم الحسي العصبي"@ar,
        "Krankheit"@de,
        "Autosomal recessive disease that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has material basis in a mutation in the endothelin B receptor gene (EDNRB)"@en,
        "condición médica"@es,
        "Doença autossômica recessiva caracterizada por albinismo, bloqueio preto, distúrbio da migração celular dos neurócitos do intestino e surdez neurossensorial, com base material em uma mutação no gene do receptor da endotelina B (EDNRB)."@pt,
        "Doença autossômica recessiva caracterizada por albinismo, bloqueio preto, distúrbio da migração celular dos neurócitos do intestino e surdez neurossensorial, com base material em uma mutação no gene do receptor da endotelina B (EDNRB)."@pt-br,
        "Медицинско стање"@sr,
        "хвороба"@uk ;
    schema1:version 2560168243 ;
    wikibase:identifiers 13 ;
    wikibase:sitelinks 8 ;
    wikibase:statements 31 ;
    skos:altLabel "ABCDS"@en,
        "ALBINISM, BLACK LOCK, CELL MIGRATION DISORDER OF THE NEUROCYTES OF THE GUT, AND DEAFNESS"@en,
        "albinism, block lock, cell migration disorder of the neurocytes of the gut, and deafness"@en,
        "Sindrome ABCD"@es,
        "Abcd, syndrome"@fr,
        "Syndrome Abcd"@fr ;
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        wds:Q3508565-EF9FF80D-F7D9-49B4-A9C1-21B734D130F3,
        wds:Q3508565-F6583439-9292-4CE4-943A-6C8B02117DCC ;
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    p:P699 wds:Q3508565-11FDFFFF-423A-4287-9B86-1AA58E22F6B2 ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/C535334> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0010895> ;
    wdtn:P6366 <https://makg.org/entity/2775853878> ;
    wdtn:P665 <http://www.kegg.jp/entry/H00823> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050600> ;
    wdt:P11430 "DI-00013" ;
    wdt:P14914 "D00918" ;
    wdt:P1550 "918" ;
    wdt:P1995 wd:Q7162 ;
    wdt:P2293 wd:Q390543 ;
    wdt:P279 wd:Q10267817,
        wd:Q56014317 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0050600>,
        <http://purl.obolibrary.org/obo/DOID_0050600> ;
    wdt:P2892 "C1838099" ;
    wdt:P31 wd:Q112193867 ;
    wdt:P3417 "ABCD-Syndrome" ;
    wdt:P486 "C535334" ;
    wdt:P492 "600501" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0010895" ;
    wdt:P557 "33683" ;
    wdt:P6366 "2775853878" ;
    wdt:P646 "/m/08nzs6" ;
    wdt:P6532 wd:Q12133,
        wd:Q1343645,
        wd:Q21953121,
        wd:Q2781245,
        wd:Q29019841,
        wd:Q55011503,
        wd:Q55781631,
        wd:Q81867,
        wd:Q933716 ;
    wdt:P665 "H00823" ;
    wdt:P699 "DOID:0050600" .