@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/715402001>
  skos:prefLabel "مقاومت ارثی گلوکوکورتیکوئید (اختلال)"@fa, "Hereditary glucocorticoid resistance (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/766817004>
  skos:prefLabel "کوتاهی قد به دلیل کمبود GHSR (گیرنده ترشح کننده هورمون رشد)."@fa, "Short stature due to GHSR (growth hormone secretagogue receptor) deficiency"@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/723362004>
  skos:prefLabel "هیپوتریکوزیس ارثی سیمپلکس (اختلال)"@fa, "Hereditary hypotrichosis simplex (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/723363009>
  skos:prefLabel "هیپوتریکوز، لنف ادم، تلانژکتازی، سندرم نقص کلیوی (اختلال)"@fa, "Hypotrichosis, lymphedema, telangiectasia, renal defect 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/783092005>
  skos:prefLabel "46، اختلال XY در رشد جنسی، نارسایی آدرنال ناشی از سیتوکروم P450 خانواده 11 زیرخانواده A عضو 1 کمبود"@fa, "46,XY disorder of sex development, adrenal insufficiency due to cytochrome P450 family 11 subfamily A member 1 deficiency"@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/763377006>
  skos:prefLabel "پاراپلژی اسپاستیک اتوزومال نوع 30 (اختلال)"@fa, "Autosomal spastic paraplegia type 30 (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/782826009>
  skos:prefLabel "بیماری Charcot Marie Tooth نوع 2P (اختلال)"@fa, "Charcot-Marie-Tooth disease type 2P (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/770726004>
  skos:prefLabel "ناباروری زنان به دلیل نقص زونا پلوسیدا (اختلال)"@fa, "Female infertility due to zona pellucida defect (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/773333003>
  skos:prefLabel "لوپوس اریتماتوز سیستمیک اتوزومال (اختلال)"@fa, "Autosomal systemic lupus erythematosus (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/764939004>
  skos:prefLabel "Fundus albipunctatus"@fa, "Fundus albipunctatus"@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/722382006>
  skos:prefLabel "آب مروارید و سندرم میکرو قرنیه (اختلال)"@fa, "Cataract and microcornea 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/782727008>
  skos:prefLabel "پاراپلژی اسپاستیک اتوزومال نوع 72"@fa, "Autosomal spastic paraplegia type 72"@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/782934004>
  skos:prefLabel "دیاتز خونریزی به دلیل نقص گیرنده کلاژن"@fa, "Bleeding diathesis due to collagen receptor defect"@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/702365002>
  skos:prefLabel "CMAMMA ترکیبی از اسیدوری مالونیک و متیل مالونیک است"@fa, "CMAMMA - combined malonic and methylmalonic aciduria"@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/784345005>
  skos:prefLabel "تشنج ناقص مهاجرت بدخیم MMPSI در دوران نوزادی"@fa, "MMPSI - malignant migrating partial seizures of infancy"@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/766929007>
  skos:prefLabel "هیپرفریتینمی ژنتیکی بدون اضافه بار آهن"@fa, "Genetic hyperferritinemia without iron overload"@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/766032007>
  skos:prefLabel "سندرم هارتسفیلد"@fa, "Hartsfield 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/783255002>
  skos:prefLabel "کم خونی آپلاستیک جدا شده ارثی"@fa, "Hereditary isolated aplastic anemia"@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/70041004>
  skos:prefLabel "اریتروکراتودرمی واریابیلیس"@fa, "Erythrokeratodermia variabilis"@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/783696009>
  skos:prefLabel "هیپرآندروژنیسم ناشی از کمبود کورتیزون ردوکتاز"@fa, "Hyperandrogenism due to cortisone reductase deficiency"@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/787413007>
  skos:prefLabel "بینی بیفید (اختلال)"@fa, "Bifid nose (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/703226008>
  skos:prefLabel "آنوریسم فامیلی ساکولار مغزی (اختلال)"@fa, "Familial cerebral saccular aneurysm (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/733467001>
  skos:prefLabel "آنتودرمی ارثی (اختلال)"@fa, "Hereditary anetoderma (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/17144009>
  skos:prefLabel "فیبروکندروژنز"@fa, "Fibrochondrogenesis"@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/783740007>
  skos:prefLabel "هیپرانسولینیسم کانونی مقاوم به دیازوکسید به دلیل کمبود SUR1"@fa, "Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency"@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/442511009>
  skos:prefLabel "انسفالوپاتی پیشرونده همراه با ادم، هیپساریتمی و سندرم آتروفی بینایی"@fa, "Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy 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/58795000>
  skos:prefLabel "دیستروفی عضلانی گوور"@fa, "Gower's muscular dystrophy"@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/723554006>
  skos:prefLabel "سندرم Oculoectodermal"@fa, "Oculoectodermal 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/722436002>
  skos:prefLabel "اپیدرمولیز دیستروفیک فقط بولوزا ناخن (اختلال)"@fa, "Dystrophic epidermolysis bullosa nails only (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/733091002>
  skos:prefLabel "فلج صورت مادرزادی ارثی (اختلال)"@fa, "Isolated hereditary congenital facial paralysis (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/773735007>
  skos:prefLabel "ناشنوایی با سندرم انیکودیستروفی"@fa, "Deafness with onychodystrophy 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/733638006>
  skos:prefLabel "اپیدرمولیز بولوزا دیستروفیک آکرال (اختلال)"@fa, "Acral dystrophic epidermolysis bullosa (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/725164008>
  skos:prefLabel "Omodysplasia (اختلال)"@fa, "Omodysplasia (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/764942005>
  skos:prefLabel "میکروفتالمی کلوبوماتوز، سندرم دیسپلازی ریزوملیک (اختلال)"@fa, "Colobomatous microphthalmia, rhizomelic dysplasia 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/723553000>
  skos:prefLabel "درمولیز بولوز گذرا نوزاد (اختلال)"@fa, "Transient bullous dermolysis of newborn (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/724351008>
  skos:prefLabel "هایپراکپلکسی ارثی (اختلال)"@fa, "Hereditary hyperekplexia (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/721172000>
  skos:prefLabel "هیپومنیزیمی همراه با نورموکلسیوری (اختلال)"@fa, "Hypomagnesemia co-occurrent with normocalciuria (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/717788000>
  skos:prefLabel "هیپومنیزیمی اولیه خانوادگی همراه با نورموکلسیوری (اختلال)"@fa, "Familial primary hypomagnesemia with normocalciuria (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/778010006>
  skos:prefLabel "شکنندگی پوست، موهای پشمی، سندرم کراتودرمی کف پلانتار (اختلال)"@fa, "Skin fragility, wooly hair, palmoplantar keratoderma 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/24269006>
  skos:prefLabel "سندرم آرتروگریپوز دیستال"@fa, "Distal arthrogryposis 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/702349003>
  skos:prefLabel "میوپاتی تجمع اکتین (اختلال)"@fa, "Actin accumulation myopathy (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/128107007>
  skos:prefLabel "بیماری فون ویلبراند نوع 2"@fa, "von Willebrand disease type 2"@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/85995004>
  skos:prefLabel "اختلال ارثی مغلوب، NOS"@fa, "Recessive 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/722458000>
  skos:prefLabel "آنوفتالمی با سندرم هیپوپلازی ریوی"@fa, "Anophthalmia with pulmonary hypoplasia 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/698870008>
  skos:prefLabel "2 اسیدوری هیدروکسی گلوتاریک"@fa, "2-hydroxyglutaric aciduria"@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/773771008>
  skos:prefLabel "نزدیک بینی جدا شده نادر"@fa, "Rare isolated myopia"@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/720601000>, <http://www.irandoc.acir/onto/irandoc/47434006>, <http://www.irandoc.acir/onto/irandoc/733091002>, <http://www.irandoc.acir/onto/irandoc/723553000>, <http://www.irandoc.acir/onto/irandoc/766817004>, <http://www.irandoc.acir/onto/irandoc/782727008>, <http://www.irandoc.acir/onto/irandoc/733467001>, <http://www.irandoc.acir/onto/irandoc/721172000>, <http://www.irandoc.acir/onto/irandoc/722458000>, <http://www.irandoc.acir/onto/irandoc/715402001>, <http://www.irandoc.acir/onto/irandoc/787413007>, <http://www.irandoc.acir/onto/irandoc/770726004>, <http://www.irandoc.acir/onto/irandoc/782826009>, <http://www.irandoc.acir/onto/irandoc/763377006>, <http://www.irandoc.acir/onto/irandoc/766032007>, <http://www.irandoc.acir/onto/irandoc/782934004>, <http://www.irandoc.acir/onto/irandoc/722382006>, <http://www.irandoc.acir/onto/irandoc/725164008>, <http://www.irandoc.acir/onto/irandoc/442511009>, <http://www.irandoc.acir/onto/irandoc/24269006>, <http://www.irandoc.acir/onto/irandoc/783255002>, <http://www.irandoc.acir/onto/irandoc/773735007>, <http://www.irandoc.acir/onto/irandoc/783696009>, <http://www.irandoc.acir/onto/irandoc/773333003>, <http://www.irandoc.acir/onto/irandoc/702365002>, <http://www.irandoc.acir/onto/irandoc/764942005>, <http://www.irandoc.acir/onto/irandoc/723362004>, <http://www.irandoc.acir/onto/irandoc/784345005>, <http://www.irandoc.acir/onto/irandoc/778010006>, <http://www.irandoc.acir/onto/irandoc/11164009>, <http://www.irandoc.acir/onto/irandoc/702349003>, <http://www.irandoc.acir/onto/irandoc/17144009>, <http://www.irandoc.acir/onto/irandoc/783740007>, <http://www.irandoc.acir/onto/irandoc/703226008>, <http://www.irandoc.acir/onto/irandoc/773728004>, <http://www.irandoc.acir/onto/irandoc/698870008>, <http://www.irandoc.acir/onto/irandoc/723554006>, <http://www.irandoc.acir/onto/irandoc/70041004>, <http://www.irandoc.acir/onto/irandoc/733638006>, <http://www.irandoc.acir/onto/irandoc/722436002>, <http://www.irandoc.acir/onto/irandoc/783092005>, <http://www.irandoc.acir/onto/irandoc/724351008>, <http://www.irandoc.acir/onto/irandoc/723363009>, <http://www.irandoc.acir/onto/irandoc/764939004>, <http://www.irandoc.acir/onto/irandoc/85995004>, <http://www.irandoc.acir/onto/irandoc/128107007>, <http://www.irandoc.acir/onto/irandoc/717788000>, <http://www.irandoc.acir/onto/irandoc/766929007>, <http://www.irandoc.acir/onto/irandoc/773771008>, <http://www.irandoc.acir/onto/irandoc/58795000> ;
  skos:prefLabel "اختلال ارثی اتوزومال"@fa, "Autosomal hereditary disorder"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  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/720601000>
  skos:prefLabel "سندرم CATSHL (کمپتوداکتیلی، قد بلند، اسکولیوز، کم شنوایی)"@fa, "CATSHL (camptodactyly, tall stature, scoliosis, hearing loss) 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> .

ns0:Is_a rdfs:label "هست یک"@fa, "Is a"@en .
<http://www.irandoc.acir/onto/irandoc/773728004>
  skos:prefLabel "کمبود گلوبولین اتصال به کورتیکواستروئید (اختلال)"@fa, "Corticosteroid-binding globulin 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> .