@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix ns0: <http://rdf-vocabulary.ddialliance.org/xkos#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .

<http://www.irandoc.acir/onto/irandoc/1208864004>
  skos:prefLabel "سندرم QT طولانی نوع 2 (اختلال)"@fa, "Long QT syndrome type 2 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/51022005>
  skos:prefLabel "پروتوپورفیری اریتروپوئیتیک"@fa, "Erythropoietic protoporphyria"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1208884000>
  skos:prefLabel "سندرم QT طولانی نوع 10 (اختلال)"@fa, "Long QT syndrome type 10 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1208863005>
  skos:prefLabel "سندرم QT طولانی نوع 5 (اختلال)"@fa, "Long QT syndrome type 5 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1208868001>
  skos:prefLabel "سندرم QT طولانی نوع 12 (اختلال)"@fa, "Long QT syndrome type 12 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/32895009>
  skos:prefLabel "بیماری ارثی"@fa, "Hereditary disease"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  skos:narrower <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1208861007>
  skos:prefLabel "سندرم QT طولانی نوع 4 (اختلال)"@fa, "Long QT syndrome type 4 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1208413008>
  skos:prefLabel "میوپاتی عدم تناسب نوع فیبر مادرزادی ناشی از جهش ACTA1"@fa, "Congenital fibre-type disproportion myopathy due to ACTA1 mutation"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/880067009>
  skos:prefLabel "بیماری بلونت"@fa, "Blount disease"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1208416000>
  skos:prefLabel "میوپاتی عدم تناسب نوع فیبر مادرزادی ناشی از جهش تروپومیوزین 3"@fa, "Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

ns0:Is_a rdfs:label "هست یک"@fa, "Is a"@en .
<http://www.irandoc.acir/onto/irandoc/1197747005>
  skos:prefLabel "لامینوپاتی لیپودیستروفیک شدید اتوزومال نیمه غالب (اختلال)"@fa, "Autosomal semi-dominant severe lipodystrophic laminopathy (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1197156008>
  skos:prefLabel "میوپاتی نمالین متوسط"@fa, "Intermediate nemaline myopathy"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/47434006>
  skos:prefLabel "سندرم وااردنبورگ"@fa, "Waardenburg's syndrome"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1208866002>
  skos:prefLabel "سندرم QT طولانی نوع 3 (اختلال)"@fa, "Long QT syndrome type 3 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1208881008>
  skos:prefLabel "سندرم QT طولانی نوع 11 (اختلال)"@fa, "Long QT syndrome type 11 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1230272009>
  skos:prefLabel "کم کاری تیروئید ناشی از جهش گیرنده TSH"@fa, "Hypothyroidism due to TSH receptor mutation"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1172637002>
  skos:prefLabel "ناباروری زنان به دلیل توقف میوز تخمک"@fa, "Female infertility due to oocyte meiotic arrest"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/11164009>
  skos:prefLabel "اختلال ارثی غالب، NOS"@fa, "Dominant hereditary disorder, NOS"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1003379004>
  skos:prefLabel "Osteogenesis imperfecta نوع V"@fa, "Osteogenesis imperfecta type V"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/442917000>
  skos:prefLabel "سندرم مادرزادی QT طولانی (اختلال)"@fa, "Congenital long QT syndrome (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1197059004>
  skos:prefLabel "ایکتیوز مادرزادی، میکروسفالی، سندرم تتراپلژی (اختلال)"@fa, "Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1197153000>
  skos:prefLabel "میوپاتی نمالینی معمولی"@fa, "Typical nemaline myopathy"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1216941002>
  skos:prefLabel "کتواسیدوز ناشی از کمبود ناقل مونوکربوکسیلات 1 (اختلال)"@fa, "Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1172696009>
  skos:prefLabel "تاخیر رشد جهانی، ناهنجاری های بینایی، آتروفی پیشرونده مخچه، سندرم هیپوتونی تنه (اختلال)"@fa, "Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1899006>
  skos:narrower <http://www.irandoc.acir/onto/irandoc/1216941002>, <http://www.irandoc.acir/onto/irandoc/1208864004>, <http://www.irandoc.acir/onto/irandoc/1208861007>, <http://www.irandoc.acir/onto/irandoc/1208866002>, <http://www.irandoc.acir/onto/irandoc/1208884000>, <http://www.irandoc.acir/onto/irandoc/1208881008>, <http://www.irandoc.acir/onto/irandoc/1187045009>, <http://www.irandoc.acir/onto/irandoc/880067009>, <http://www.irandoc.acir/onto/irandoc/1230272009>, <http://www.irandoc.acir/onto/irandoc/1172696009>, <http://www.irandoc.acir/onto/irandoc/1208870005>, <http://www.irandoc.acir/onto/irandoc/1208863005>, <http://www.irandoc.acir/onto/irandoc/1208416000>, <http://www.irandoc.acir/onto/irandoc/1197059004>, <http://www.irandoc.acir/onto/irandoc/1201863001>, <http://www.irandoc.acir/onto/irandoc/1208868001>, <http://www.irandoc.acir/onto/irandoc/47434006>, <http://www.irandoc.acir/onto/irandoc/1197153000>, <http://www.irandoc.acir/onto/irandoc/11164009>, <http://www.irandoc.acir/onto/irandoc/1208413008>, <http://www.irandoc.acir/onto/irandoc/702444009>, <http://www.irandoc.acir/onto/irandoc/442917000>, <http://www.irandoc.acir/onto/irandoc/1172637002>, <http://www.irandoc.acir/onto/irandoc/1197156008>, <http://www.irandoc.acir/onto/irandoc/1197747005>, <http://www.irandoc.acir/onto/irandoc/1003379004>, <http://www.irandoc.acir/onto/irandoc/51022005> ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  skos:prefLabel "اختلال ارثی اتوزومال"@fa, "Autosomal hereditary disorder"@en ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/32895009> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/32895009> .

<http://www.irandoc.acir/onto/irandoc/1201863001>
  skos:prefLabel "اسکلروز جانبی آمیوتروفیک نوع 1"@fa, "Amyotrophic lateral sclerosis type 1"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1187045009>
  skos:prefLabel "سندرم Aicardi Goutieres نوع 1"@fa, "Aicardi Goutieres syndrome type 1"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/1208870005>
  skos:prefLabel "سندرم QT طولانی نوع 13 (اختلال)"@fa, "Long QT syndrome type 13 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .

<http://www.irandoc.acir/onto/irandoc/702444009>
  skos:prefLabel "سندرم لنفوپرولیفراتیو خود ایمنی"@fa, "Autoimmune lymphoproliferative syndrome"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/1899006> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/1899006> .