@prefix vh8: <http://data.loterre.fr/ark:/67375/VH8> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .

vh8:-RTDFFD77-F
  skos:prefLabel "syndrome de Haber"@fr, "Haber syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JSZKFZXV-Q
  skos:prefLabel "short QT syndrome"@en, "syndrome du QT court"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PJQJX191-B
  skos:prefLabel "syndrome des glycoprotéines déficientes en hydrates de carbone"@fr, "carbohydrate deficient glycoprotein syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-X43ZHQLR-L
  skos:prefLabel "Holt-Oram syndrome"@en, "syndrome de Holt-Oram"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-S9L9G8F0-C
  skos:prefLabel "hyperphosphatasie"@fr, "hyperphosphatasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-W9C0N9B0-2
  skos:prefLabel "fragile X-associated tremor/ataxia syndrome"@en, "syndrome des tremblements ataxiques associé au X fragile"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RJPT8CP6-9
  skos:prefLabel "Nijmegen breakage syndrome"@en, "syndrome de Nimègue"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KXN51K6K-L
  skos:prefLabel "syndrome de Reifenstein"@fr, "Reifenstein syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NH2B8Q57-Z
  skos:prefLabel "kératome malin diffus congénital"@fr, "malignant keratoma"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XJP1R0N1-0
  skos:prefLabel "épidermolyse bulleuse dystrophique"@fr, "dystrophic epidermolysis bullosa"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HVD7R058-H
  skos:prefLabel "ostéolyse expansive familiale"@fr, "familial expansile osteolysis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HPQHHQFN-C
  skos:prefLabel "syndrome H"@fr, "H syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TCTTWJHS-0
  skos:prefLabel "hyperkalemic periodic paralysis"@en, "paralysie périodique hyperkaliémique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HTND2FS7-5
  skos:prefLabel "Chediak syndrome"@en, "maladie de Chediak"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NZNJ4N5X-1
  skos:prefLabel "déficit en hypoxanthine-guanine phosphoribosyltransférase"@fr, "hypoxanthine-guanine phosphoribosyltransferase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-L0JL9X6F-K
  skos:prefLabel "Dorfman-Chanarin syndrome"@en, "syndrome de Dorfman-Chanarin"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-H61CCVXJ-9
  skos:prefLabel "Carney complex"@en, "complexe de Carney"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DSKXXC3N-B
  skos:prefLabel "dyschromatosis universalis hereditaria"@en, "dyschromatose universelle"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-D8ZHWSJC-S
  skos:prefLabel "cleidocranial dysplasia"@en, "dysplasie cléidocrânienne"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-S022433K-R
  skos:prefLabel "fièvre méditerranéenne familiale"@fr, "familial recurrent polyseritis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SP5NMVCZ-1
  skos:prefLabel "ataxia telangiectasia"@en, "ataxie télangiectasie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QBDZS657-P
  skos:prefLabel "amaurose congénitale de Leber"@fr, "Leber amaurosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-C9RF54DZ-5
  skos:prefLabel "Li-Fraumeni syndrome"@en, "syndrome de Li-Fraumeni"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HTHZBLS6-0
  skos:prefLabel "diabète MODY"@fr, "maturity onset diabetes of the young"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-P5X7C1GC-0
  skos:prefLabel "hyalinosis cutis et mucosae"@en, "hyalinose cutanéomuqueuse"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MG40KRBS-4
  skos:prefLabel "syndrome de Rieger"@fr, "iridocorneal mesodermal dysgenesis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-N0JB9FMQ-0
  skos:prefLabel "immunodéficit héréditaire DiGeorge"@fr, "DiGeorge syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-B35NZ4NM-2
  skos:prefLabel "syndrome de Jadassohn-Lewandowsky"@fr, "Jadassohn-Lewandowsky syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KD24XNHG-0
  skos:prefLabel "Bourneville syndrome"@en, "phacomatose de Bourneville"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BGHF6WV3-R
  skos:prefLabel "multiple endocrine neoplasia type II"@en, "polyadénomatose endocrinienne de type II"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XMV0VNPM-3
  skos:prefLabel "maladie polykystique hépatorénale"@fr, "polycystic hepatorenal disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-T0PXSL0G-0
  skos:prefLabel "Norrie disease"@en, "cécité héréditaire de Norrie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-K0VM4SGQ-9
  skos:prefLabel "amélogenèse imparfaite"@fr, "amelogenesis imperfecta"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PG2JQKF2-L
  skos:prefLabel "dégénérescence pigmentaire en aile de papillon"@fr, "butterfly shaped pigment degeneration"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CBB68715-4
  skos:prefLabel "Pallister-Hall syndrome"@en, "syndrome de Pallister-Hall"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-R5KHXLC9-1
  skos:prefLabel "Werdnig-Hoffmann disease"@en, "amyotrophie de Werdnig-Hoffmann"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RJ974JGR-X
  skos:prefLabel "syndrome de Comèl-Netherton"@fr, "Comel-Netherton syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BTC4V8S3-Z
  skos:prefLabel "épidermolyse bulleuse létale"@fr, "epidermolysis bullosa hereditaria letalis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZMWF2DVC-D
  skos:prefLabel "syndrome de Noonan"@fr, "Noonan syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TZPCK8FB-G
  skos:prefLabel "chondrodysplasie type Grebe"@fr, "Grebe type chondrodysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BR24NLLD-X
  skos:prefLabel "syndrome CADASIL"@fr, "CADASIL syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SJC71XJ0-D
  skos:prefLabel "dystrophie cornéenne granulaire"@fr, "granular corneal dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HV46RFL7-X
  skos:prefLabel "kératodermie palmoplantaire et périorificielle d'Olmsted"@fr, "mutilating palmoplantar keratoderma with periorificial keratotic plaques"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-M4J6FDR7-3
  skos:prefLabel "syndrome blépharo-cheilo-odontique"@fr, "blepharo-cheilo-odontic syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SWB1KGJ3-W
  skos:prefLabel "dermatofibrose lenticulaire disséminée"@fr, "disseminated lenticular dermatofibrosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-P1Q80MJ2-3
  skos:prefLabel "syndrome trichorhinophalangien"@fr, "trichorhinophalangeal syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XZ4ZJWSL-L
  skos:prefLabel "syndrome hydrolethalus"@fr, "hydrolethalus syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-C4NHTKSL-L
  skos:prefLabel "érythrodermie ichtyosiforme bulleuse"@fr, "bullous ichtyosiform erythroderma"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TRNJ5V7P-R
  skos:prefLabel "white sponge nevus"@en, "naevus blanc spongieux"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KSS0VVWV-B
  skos:prefLabel "dysostose mandibulofaciale"@fr, "mandibulofacial dysostosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MVHXVZHT-W
  skos:prefLabel "dysplasie pseudoachondroplasique"@fr, "pseudoachondroplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KGGZ06WD-G
  skos:prefLabel "lipoprotein lipase deficiency"@en, "déficit en lipoprotéine lipase"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZWW7QBD6-G
  skos:prefLabel "syndrome du cil immobile"@fr, "immotile cilia syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Z5XTW2TT-T
  skos:prefLabel "nanisme de Smith-Lemli-Opitz"@fr, "Smith-Lemli-Opitz dwarfism"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-LJ780PM6-N
  skos:prefLabel "foie polykystique"@fr, "polycystic liver"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TP6S617R-0
  skos:prefLabel "lentiginose centrofaciale de Touraine"@fr, "Touraine centrofacial lentiginosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BXHLV6LV-R
  skos:prefLabel "cylindrome de Brooke Spiegler"@fr, "Brooke-Spiegler cylindroma"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-T9L0CKN1-D
  skos:prefLabel "Rotor disease"@en, "ictère héréditaire de Rotor"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CRQ2TNWZ-K
  skos:prefLabel "galactosemia"@en, "galactosémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HKMXSRPZ-H
  skos:prefLabel "dysplasie polyépiphysaire dominante"@fr, "dominant multiple epiphyseal dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-P9GV521K-5
  skos:prefLabel "syndrome de Cowden"@fr, "Cowden syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-X8PGNTR2-N
  skos:prefLabel "sclerosteosis"@en, "sclérostéose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DF27RSF5-D
  skos:prefLabel "hyperoxalurie"@fr, "hyperoxaluria"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MV0MMSMP-W
  skos:prefLabel "immunodéficit combiné"@fr, "combined immune deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-H2B6QNR7-B
  skos:prefLabel "porphyrie"@fr, "porphyria"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NXBXDZWS-R
  skos:prefLabel "Pelizaeus–Merzbacher disease"@en, "maladie de Pelizaeus-Merzbacher"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SMS1K39H-4
  skos:prefLabel "Marinesco-Sjögren syndrome"@en, "syndrome de Marinesco-Sjögren"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BGL2ZJ6Q-M
  skos:prefLabel "syndrome d'Ehlers-Danlos"@fr, "Ehlers-Danlos syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BN52NFFK-X
  skos:prefLabel "diastrophic dysplasia"@en, "nanisme diastrophique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Z70D31CR-F
  skos:prefLabel "polycystic kidney"@en, "rein polykystique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-G0RDHRV9-X
  skos:prefLabel "syndrome de Winchester"@fr, "Winchester syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-LR08XW6J-X
  skos:prefLabel "diarrhée chlorée congénitale"@fr, "congenital chloride diarrhea"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MLT3S87P-K
  skos:prefLabel "syndrome de Galloway"@fr, "Galloway syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-K8NL2XBB-F
  skos:prefLabel "dysplasie ventriculaire droite arythmogène"@fr, "arrhythmogenic right ventricular dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XPPL5JKV-R
  skos:prefLabel "vitréorétinopathie exsudative familiale"@fr, "familial exsudative vitreoretinopathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DJJXC0KJ-V
  skos:prefLabel "rétinoschisis idiopathique juvénile"@fr, "juvenile retinoschisis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QM458V2K-L
  skos:prefLabel "pyropoikilocytose héréditaire"@fr, "piropoikilocytosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-G88QPTXP-C
  skos:prefLabel "maladie de Segawa"@fr, "Segawa disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-H5J0LWV2-F
  skos:prefLabel "von Hippel-Lindau disease"@en, "angiomatose cérébellorétinienne de von Hippel-Lindau"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JNQ5NT8R-2
  skos:prefLabel "syndrome SAMS"@fr, "SAMS syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-F34S0VJB-T
  skos:prefLabel "aminoacidurie rénale"@fr, "hereditary tubulopathy aminoaciduria"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BB6SW476-B
  skos:prefLabel "neuroaxonal dystrophy"@en, "dystrophie neuroaxonale"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-K4G2JJ0L-5
  skos:prefLabel "dystrophie musculaire"@fr, "muscular dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PJP86JDT-L
  skos:prefLabel "rétinopathie cristalline de Bietti"@fr, "Bietti crystalline retinopathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PLPSC0WL-4
  skos:prefLabel "oxalose"@fr, "oxalosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-W234BP90-T
  skos:prefLabel "maladie du cri du chat"@fr, "cri du chat syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-LB6QSBT5-Z
  skos:prefLabel "Buschke-Fischer's keratoderma"@en, "kératodermie verrucoïde de Buschke-Fischer"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-C45KVQF0-5
  skos:prefLabel "recessive multiple epiphyseal dysplasia"@en, "dysplasie polyépiphysaire récessive"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QBHNZVRZ-P
  skos:prefLabel "xeroderma pigmentosum"@fr, "xeroderma pigmentosum"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-FSSTTC7P-C
  skos:prefLabel "incontinentia pigmenti"@fr, "incontinentia pigmenti"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-FSJR16PS-C
  skos:prefLabel "syndrome de Gitelmann"@fr, "Gitelman syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-T33HR75Z-G
  skos:prefLabel "trichothiodystrophie"@fr, "trichothiodystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GKM0J6RV-N
  skos:prefLabel "extrémités en pince de homard"@fr, "split-hand split-foot syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GDK10NVJ-F
  skos:prefLabel "ictère héréditaire de Gilbert"@fr, "Gilbert disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-M1L4VZ8H-1
  skos:prefLabel "dystrophie cornéenne de Groenouw type I"@fr, "Groenouw type I corneal dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MGG0QRPT-S
  skos:prefLabel "pyruvate kinase deficiency"@en, "déficit en pyruvate kinase"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-F8BNBFKN-6
  skos:prefLabel "syndrome de Mohr"@fr, "Mohr syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QL05HT4M-3
  skos:prefLabel "hereditary mucoepithelial dysplasia"@en, "dysplasie mucoépithéliale héréditaire"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QQKF2GK3-J
  skos:prefLabel "syndrome d'excès apparent de minéralocorticoïde"@fr, "apparent mineralocorticoid excess syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-FZ8NKM7M-5
  skos:prefLabel "rétinite pigmentaire"@fr, "retinitis pigmentosa"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JJX4NJBN-4
  skos:prefLabel "osteogenesis imperfecta"@en, "ostéogenèse imparfaite"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QRCTQWM2-Q
  skos:prefLabel "Kugelberg-Welander disease"@en, "amyotrophie de Kugelberg-Welander"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-G3FN99NS-0
  skos:prefLabel "épidermolyse bulleuse jonctionnelle"@fr, "junctional epidermolysis bullosa"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-H65V5PX7-9
  skos:prefLabel "hypophosphatasie"@fr, "hypophosphatasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PRSSL1XP-5
  skos:prefLabel "thésaurismose"@fr, "storage disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-W7JQXDDR-W
  skos:prefLabel "Usher syndrome"@en, "syndrome d'Usher"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SPNL2Z1Z-P
  skos:prefLabel "abêtalipoprotéinémie"@fr, "abetalipoproteinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DGKNJWH1-J
  skos:prefLabel "dystonie musculaire déformante"@fr, "dystonia musculorum deformans"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GQ6VT558-G
  skos:prefLabel "pseudohypoparathyroïdie"@fr, "pseudohypoparathyroidism"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BFFB02NN-7
  skos:prefLabel "comédon dyskératosique familial"@fr, "familial dyskeratotic comedones"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-V89H430T-7
  skos:prefLabel "syndrome laryngo-onycho-cutané"@fr, "laryngo-onycho-cutaneous syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Q6G3GCHC-W
  skos:prefLabel "dermopathie restrictive"@fr, "restrictive dermopathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BHTSG3ZT-D
  skos:prefLabel "ostéodysplasie métaphysaire de Pyle"@fr, "Pyle metaphyseal dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-VPRSJ3L9-M
  skos:prefLabel "Divry-van Bogaert disease"@en, "angiomatose neurocutanée de Divry-van Bogaert"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-M91FVLZ5-3
  skos:prefLabel "hypoplasie dermique en aires"@fr, "focal dermal hypoplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-F4XWZFKN-T
  skos:prefLabel "lipodystrophie de Berardinelli"@fr, "Berardinelli lipodystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RM7L6Z6J-L
  skos:prefLabel "Shwachman-Diamond syndrome"@en, "syndrome de Shwachman-Diamond"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-P6XNB1R1-2
  skos:prefLabel "hyperthyroxinémie dysalbuminémique familiale"@fr, "familial dysalbuminemic hyperthyroxinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZSV003ZN-V
  skos:prefLabel "pachydermoperiostosis"@en, "pachydermopériostose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZZ603TW5-M
  skos:prefLabel "Melnick-Fraser syndrome"@en, "syndrome de Melnick-Fraser"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JJQ21H5D-L
  skos:prefLabel "hémoglobine instable"@fr, "unstable hemoglobin"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CPZWLRSQ-B
  skos:prefLabel "leukocyte adhesion deficiency"@en, "déficit d'adhérence leucocytaire"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-N1XLFSWL-0
  skos:prefLabel "acropigmentation de Dohi"@fr, "Dohi acropigmentation"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PWW2NTBX-L
  skos:prefLabel "dystrophie cornéenne grillagée"@fr, "lattice corneal dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-D37TBS59-N
  skos:prefLabel "stiff skin syndrome"@en, "syndrome de la peau cartonnée"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KK63SMWR-X
  skos:prefLabel "hypoalphalipoproteinemia"@en, "hypoalphalipoprotéinémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JL0VPXFQ-6
  skos:prefLabel "multiple endocrine neoplasia type I"@en, "polyadénomatose endocrinienne de type I"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-FHDLVS0M-7
  skos:prefLabel "alpha-1 antitrypsin deficiency"@en, "déficit en alpha-1 antitrypsine"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JC691V5L-D
  skos:prefLabel "chondrodysplasie métaphysaire"@fr, "metaphyseal chondrodysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-M76LFNL3-8
  skos:prefLabel "insomnie familiale fatale"@fr, "fatal familial insomnia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-J0JMX5B1-X
  skos:prefLabel "De Barsy syndrome"@en, "syndrome de De Barsy"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BJ3GRX9W-9
  skos:prefLabel "Charcot-Marie-Tooth disease"@en, "amyotrophie de Charcot-Marie-Tooth"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-G5JJQ282-0
  skos:prefLabel "dystrophie cornéenne de Meesmann"@fr, "Meesmann corneal dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NV617XJD-T
  skos:prefLabel "syndrome de Bannayan-Riley-Ruvalcaba"@fr, "Bannayan-Riley-Ruvalcaba syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-N32K7HZ8-D
  skos:narrower vh8:-MGG0QRPT-S, vh8:-JJX4NJBN-4, vh8:-LJ780PM6-N, vh8:-HLG1B0Z1-X, vh8:-GX8GZ9N5-M, vh8:-HS90PV3R-J, vh8:-ZZD1C200-G, vh8:-RJW9T491-2, vh8:-C45KVQF0-5, vh8:-QBDZS657-P, vh8:-TCTTWJHS-0, vh8:-H1M3H8ZH-Q, vh8:-QBHNZVRZ-P, vh8:-K20GGS3P-0, vh8:-RJ2ZBSVM-H, vh8:-J1Z30DNL-R, vh8:-NM3KPZ36-3, vh8:-T0PXSL0G-0, vh8:-ZJL9FB4V-2, vh8:-RR65K06J-2, vh8:-R8Q90Z0M-K, vh8:-XH4T4TXW-2, vh8:-DBTWL329-M, vh8:-G3FN99NS-0, vh8:-J0B3L2K5-M, vh8:-SL15DT0X-7, vh8:-GWPN610V-5, vh8:-JLP435RW-F, vh8:-NJGR5JGK-1, vh8:-DVDBBVQP-8, vh8:-GPZR4BFS-X, vh8:-ZSV003ZN-V, vh8:-D8ZHWSJC-S, vh8:-PSXV65MW-6, vh8:-Q653J5H2-Q, vh8:-KP5HLW1D-9, vh8:-TP6S617R-0, vh8:-P7496B13-S, vh8:-NXBXDZWS-R, vh8:-ZWPG9CNS-H, vh8:-M62V5ZC2-F, vh8:-Z3BPTXLF-D, vh8:-Z8TNPKTB-2, vh8:-J269W40Z-H, vh8:-X1NTCLP9-2, vh8:-JNB3KF12-G, vh8:-LLM7LN8S-W, vh8:-H5J0LWV2-F, vh8:-HMBMF79B-M, vh8:-PG2JQKF2-L, vh8:-XQ46WQ16-B, vh8:-B3BK074Z-V, vh8:-G0RDHRV9-X, vh8:-QL05HT4M-3, vh8:-C9RF54DZ-5, vh8:-XDR2MLWZ-3, vh8:-BGHF6WV3-R, vh8:-WK6210CD-T, vh8:-BTC4V8S3-Z, vh8:-JNP3VNPD-S, vh8:-LF9N3HBV-S, vh8:-RT94LQHJ-1, vh8:-N5XDC60G-5, vh8:-V89H430T-7, vh8:-P5X7C1GC-0, vh8:-TBFG377G-X, vh8:-SP5NMVCZ-1, vh8:-M1L4VZ8H-1, vh8:-GJHJZGMJ-H, vh8:-GM7NCGPT-9, vh8:-CF6528NT-R, vh8:-SC0DL7FZ-9, vh8:-XG4MLTB9-J, vh8:-LR08XW6J-X, vh8:-SQP1G8VG-7, vh8:-GR5FH5ZZ-7, vh8:-F4XWZFKN-T, vh8:-HPQHHQFN-C, vh8:-BBM4PRQT-B, vh8:-PRSSL1XP-5, vh8:-HTHZBLS6-0, vh8:-SPKJ93WT-3, vh8:-RRMB4HWN-T, vh8:-W234BP90-T, vh8:-H65V5PX7-9, vh8:-ZWPVBTF0-1, vh8:-CQBS1P5B-7, vh8:-KR00WQ46-J, vh8:-JNQ5NT8R-2, vh8:-K7VT1XWZ-R, vh8:-X9VP93T2-D, vh8:-XWQ6GL32-W, vh8:-JG6GHJDH-F, vh8:-HJ0D3XSC-S, vh8:-CX829SPQ-C, vh8:-QQKF2GK3-J, vh8:-TZPCK8FB-G, vh8:-M76LFNL3-8, vh8:-PJQHTX8P-6, vh8:-MWJQS8SL-Z, vh8:-GX96ZXV2-2, vh8:-HKMXSRPZ-H, vh8:-PZRZP92R-P, vh8:-K5MR1S4D-Z, vh8:-TLXPW7RJ-5, vh8:-VHSZS195-R, vh8:-XLTT5ZKK-3, vh8:-K0VM4SGQ-9, vh8:-VPRSJ3L9-M, vh8:-QTVB01PR-K, vh8:-Q8WQLCSG-F, vh8:-C83NFMMK-S, vh8:-BC56H2HC-P, vh8:-SMS1K39H-4, vh8:-ZWW7QBD6-G, vh8:-VRW6TJKT-W, vh8:-V14901J6-2, vh8:-H3GFR5RJ-9, vh8:-SV79FDHT-5, vh8:-GGHSK0G4-8, vh8:-HTTHXG7P-C, vh8:-DP7GL2QD-3, vh8:-R5P5V29B-C, vh8:-S18P65KH-F, vh8:-SWB1KGJ3-W, vh8:-XQD1VXL1-4, vh8:-M91FVLZ5-3, vh8:-XBJ2RJ3G-X, vh8:-VBXFRXMW-4, vh8:-P1Q80MJ2-3, vh8:-M38WFJ45-V, vh8:-H2T8C940-R, vh8:-HQ5GX46Z-X, vh8:-KSS0VVWV-B, vh8:-GDK10NVJ-F, vh8:-XZ4ZJWSL-L, vh8:-XDGV3JXT-H, vh8:-M8W0T5JK-9, vh8:-N1KTD1PV-S, vh8:-N0JB9FMQ-0, vh8:-HF3P255K-H, vh8:-QV88W309-T, vh8:-P9GV521K-5, vh8:-RZR694NR-W, vh8:-VSN2N43D-R, vh8:-CBB68715-4, vh8:-JL0VPXFQ-6, vh8:-RJPT8CP6-9, vh8:-KJ9T4V22-Q, vh8:-N1XLFSWL-0, vh8:-HVD7R058-H, vh8:-P334XDL2-J, vh8:-LHRLMTG3-J, vh8:-GRQJ2NXX-N, vh8:-MJMJNMFR-1, vh8:-S05JP84K-0, vh8:-KVW1ZTSK-3, vh8:-W8K8J6P8-3, vh8:-B75HKZZG-F, vh8:-BHTSG3ZT-D, vh8:-CCDM750J-8, vh8:-XS1XJPNX-C, vh8:-WQHMLFJJ-0, vh8:-Z277690J-S, vh8:-W7B3GJ02-T, vh8:-NLJ9SXMF-5, vh8:-SBKF1MC3-7, vh8:-NS40662M-D, vh8:-LB6QSBT5-Z, vh8:-MV0MMSMP-W, vh8:-D6XMQL01-N, vh8:-DJJXC0KJ-V, vh8:-Q6G3GCHC-W, vh8:-L642B2PF-3, vh8:-C4NHTKSL-L, vh8:-T61T6GTF-R, vh8:-BFFB02NN-7, vh8:-HKGCMTHZ-W, vh8:-XMV0VNPM-3, vh8:-R1JPP52M-8, vh8:-XT342XNG-R, vh8:-V5K9J0X9-P, vh8:-J0JMX5B1-X, vh8:-T33HR75Z-G, vh8:-GFV9Z0SW-R, vh8:-MNZF53TT-J, vh8:-W790N3DT-N, vh8:-H36XRD0P-V, vh8:-LBB5Q6C9-R, vh8:-J7MPXHB1-Z, vh8:-BJ3GRX9W-9, vh8:-W1LMNLHN-2, vh8:-MG9TNC4F-Q, vh8:-T45BF7ZD-G, vh8:-P386QDNJ-H, vh8:-SKNDPF65-C, vh8:-KN9CVK4Z-N, vh8:-H2B6QNR7-B, vh8:-BXHLV6LV-R, vh8:-DSV7960J-H, vh8:-DTGT58D2-K, vh8:-R5S69L9R-M, vh8:-D48QVGJZ-0, vh8:-ZZBM5ZLH-8, vh8:-NZNJ4N5X-1, vh8:-ZXDHHJBR-6, vh8:-DVC9HSRR-7, vh8:-ZMWF2DVC-D, vh8:-Z5XTW2TT-T, vh8:-JTSMWJJB-7, vh8:-NV617XJD-T, vh8:-ZFX15Q0F-G, vh8:-W9C0N9B0-2, vh8:-PLPSC0WL-4, vh8:-B2GCPK9C-8, vh8:-XZ07C46K-C, vh8:-JCFFTMRR-R, vh8:-KJJT05TH-D, vh8:-KD24XNHG-0, vh8:-FKN242QL-T, vh8:-BVT3K702-Q, vh8:-ZH5LH0DW-C, vh8:-PFH90FG8-8, vh8:-N2M310PZ-W, vh8:-X43ZHQLR-L, vh8:-WQSD96RM-H, vh8:-ZLVS4FGJ-R, vh8:-W7JQXDDR-W, vh8:-N95H3PMJ-5, vh8:-F8BNBFKN-6, vh8:-MVHXVZHT-W, vh8:-XPPL5JKV-R, vh8:-TKPTT4NP-M, vh8:-ZN8MGQFL-6, vh8:-HV46RFL7-X, vh8:-JBD14MNL-G, vh8:-G9BHQL64-S, vh8:-CPZWLRSQ-B, vh8:-R5KHXLC9-1, vh8:-X8PGNTR2-N, vh8:-CVM0W1X9-M, vh8:-JSZKFZXV-Q, vh8:-PTSX3DN0-2, vh8:-SPNL2Z1Z-P, vh8:-GZT00M67-Z, vh8:-TTMRPWR0-Q, vh8:-GF8SW923-W, vh8:-DF27RSF5-D, vh8:-VXSP9WQJ-7, vh8:-QD9ZH73G-M, vh8:-B9PQQH41-T, vh8:-ZG9NH0MB-2, vh8:-CZ8P4KQX-K, vh8:-MTJ4WC97-3, vh8:-QBC2HGP5-9, vh8:-FP8QQPSH-1, vh8:-RM7L6Z6J-L, vh8:-XJP1R0N1-0, vh8:-KN1MVJP1-7, vh8:-DSKXXC3N-B, vh8:-K7S5JQ62-3, vh8:-LCGB1PF6-2, vh8:-D7J8KX7R-Q, vh8:-Z1VGJVHN-6, vh8:-XVNKP097-D, vh8:-NFWCC1N5-Q, vh8:-BN52NFFK-X, vh8:-RVZ3P800-W, vh8:-KXN51K6K-L, vh8:-PV3JPGZL-Q, vh8:-M0N4TKT5-W, vh8:-H61CCVXJ-9, vh8:-M4J6FDR7-3, vh8:-QM458V2K-L, vh8:-JHD0JQ5Q-T, vh8:-HHHKG0B9-B, vh8:-CF4BP8DP-G, vh8:-F34S0VJB-T, vh8:-JJQ21H5D-L, vh8:-X4VG7PC6-6, vh8:-ZK7F993P-4, vh8:-D4VR1G17-D, vh8:-PWW2NTBX-L, vh8:-G5JJQ282-0, vh8:-MG40KRBS-4, vh8:-WN2FQ7Q3-5, vh8:-F42NJZ40-Z, vh8:-TRNJ5V7P-R, vh8:-BB6SW476-B, vh8:-L0JL9X6F-K, vh8:-S6VW9FXT-P, vh8:-JDT0QQQF-H, vh8:-KGGZ06WD-G, vh8:-HKHNT5BS-P, vh8:-XJWS2TVS-P, vh8:-HTND2FS7-5, vh8:-QZGXZRM9-2, vh8:-KFMBC1PX-2, vh8:-MV6JS6DZ-T, vh8:-KHS10THT-8, vh8:-W9GR1T8Z-Q, vh8:-GQ6VT558-G, vh8:-CW64S69F-2, vh8:-T9L0CKN1-D, vh8:-DRV5RGX9-R, vh8:-BR24NLLD-X, vh8:-CQWDC3HQ-X, vh8:-N5WN3GNF-S, vh8:-KF3BT8JV-H, vh8:-QLJFKDL6-9, vh8:-C7VVC7BW-N, vh8:-G88QPTXP-C, vh8:-GKM0J6RV-N, vh8:-BGL2ZJ6Q-M, vh8:-JC4ZPGWW-B, vh8:-KK63SMWR-X, vh8:-WCRT6QVG-G, vh8:-JC691V5L-D, vh8:-K17D2MN5-2, vh8:-X6PZ6KSL-3, vh8:-BZTPCQN7-B, vh8:-K4G2JJ0L-5, vh8:-BFBZPS8B-W, vh8:-G5MZL975-B, vh8:-FHDLVS0M-7, vh8:-RTDFFD77-F, vh8:-VZWLPPRV-W, vh8:-FSJR16PS-C, vh8:-ZZ603TW5-M, vh8:-NNRXM04Z-V, vh8:-TRJ1SD09-W, vh8:-JL5T2HJT-9, vh8:-CV5K91ZR-G, vh8:-SJC71XJ0-D, vh8:-C2L49H54-K, vh8:-QRCTQWM2-Q, vh8:-JVL4WG1X-L, vh8:-S9L9G8F0-C, vh8:-JXQ8RQGJ-F, vh8:-L6N8134K-9, vh8:-ZP4Q2ST6-8, vh8:-X41QB0LX-K, vh8:-XDQ7FV5D-L, vh8:-K8NL2XBB-F, vh8:-WWVN4096-B, vh8:-GJ4RDHFJ-9, vh8:-K52TXF4H-M, vh8:-RPTCZ103-Z, vh8:-DGKNJWH1-J, vh8:-QSC6VGW6-8, vh8:-S9QKFL4R-P, vh8:-ZQTHM36F-K, vh8:-RPL8R9P9-Z, vh8:-FSSTTC7P-C, vh8:-N3TGF2N9-V, vh8:-XQ683CNX-W, vh8:-NNQK6Q6W-G, vh8:-XZRTHT6F-V, vh8:-ZCRJQ7JS-B, vh8:-SQWVFPJK-2, vh8:-P6XNB1R1-2, vh8:-NH2B8Q57-Z, vh8:-TDNL9X15-P, vh8:-RJ974JGR-X, vh8:-S022433K-R, vh8:-Z5DZXH85-7, vh8:-FRHTZJFN-6, vh8:-QB7RMT32-K, vh8:-CRQ2TNWZ-K, vh8:-PJQJX191-B, vh8:-JHH6X500-H, vh8:-T6WMQ6XX-B, vh8:-VBF7D9B9-9, vh8:-F9VTM7K5-T, vh8:-MLT3S87P-K, vh8:-RD0N82HM-J, vh8:-JH4LRLKJ-0, vh8:-B9TWB15L-V, vh8:-P9Q0F9M2-F, vh8:-QT9GTQ4N-0, vh8:-BR640GJ1-S, vh8:-D37TBS59-N, vh8:-PJP86JDT-L, vh8:-FNQPCVKH-R, vh8:-B35NZ4NM-2, vh8:-Z70D31CR-F, vh8:-FZ8NKM7M-5, vh8:-Z2B6G9GP-W ;
  a skos:Concept ;
  skos:broader vh8:-CR27D8H3-X ;
  skos:prefLabel "maladie héréditaire"@fr, "hereditary disease"@en ;
  skos:inScheme vh8: .

vh8: a skos:ConceptScheme .
vh8:-Q8WQLCSG-F
  skos:prefLabel "McLeod syndrome"@en, "syndrome de McLeod"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XS1XJPNX-C
  skos:prefLabel "Papillon-Lefèvre's syndrome"@en, "kératodermie palmoplantaire de Papillon-Lefèvre"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RPL8R9P9-Z
  skos:prefLabel "lysosomal storage disease"@en, "pathologie des lysosomes"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NNRXM04Z-V
  skos:prefLabel "dysplasie rhinotrichophalangienne"@fr, "trichorhinophalangeal dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-B9PQQH41-T
  skos:prefLabel "déficit génétique du complément"@fr, "genetic complement deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-T61T6GTF-R
  skos:prefLabel "polyadénomatose endocrinienne"@fr, "multiple endocrine neoplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XLTT5ZKK-3
  skos:prefLabel "otosclerosis"@en, "otospongiose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NM3KPZ36-3
  skos:prefLabel "syndrome de Sjögren et Larsson"@fr, "Sjögren-Larsson syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SQP1G8VG-7
  skos:prefLabel "Kennedy's disease"@en, "maladie de Kennedy"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZJL9FB4V-2
  skos:prefLabel "dystrophie réticulaire pigmentaire de Sjögren"@fr, "Sjögren reticular dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RZR694NR-W
  skos:prefLabel "syndrome de Watson"@fr, "Watson syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-H36XRD0P-V
  skos:prefLabel "basal cell nevus syndrome"@en, "syndrome du naevus basocellulaire"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TLXPW7RJ-5
  skos:prefLabel "asphyxiating thoracic dysplasia"@en, "dysplasie thoracique asphyxiante"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JLP435RW-F
  skos:prefLabel "syndrome de Van der Woude"@fr, "Van der Woude syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XJWS2TVS-P
  skos:prefLabel "dyskeratosis congenita"@en, "syndrome de Zinsser-Engman-Cole"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DP7GL2QD-3
  skos:prefLabel "epidermodysplasia verruciformis"@en, "épidermodysplasie verruciforme de Lewandowsky-Lutz"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-P386QDNJ-H
  skos:prefLabel "syndrome de Wolfram"@fr, "Wolfram syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SC0DL7FZ-9
  skos:prefLabel "ictère héréditaire de Dubin-Johnson"@fr, "Dubin-Johnson disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JCFFTMRR-R
  skos:prefLabel "dégénérescence vitréorétinienne de Wagner"@fr, "Wagner vitroretinal degeneration"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZH5LH0DW-C
  skos:prefLabel "urticaire familiale au froid"@fr, "familial cold urticaria"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-S05JP84K-0
  skos:prefLabel "hypoplasminogénémie"@fr, "hypoplasminogenemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-WCRT6QVG-G
  skos:prefLabel "fucosidose"@fr, "fucosidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-S9QKFL4R-P
  skos:prefLabel "syndrome de Peters"@fr, "Peters syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XBJ2RJ3G-X
  skos:prefLabel "mucopolysaccharidosis"@en, "mucopolysaccharidose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZG9NH0MB-2
  skos:prefLabel "pathologie des peroxysomes"@fr, "peroxisomal disorders"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XDR2MLWZ-3
  skos:prefLabel "pyknodysostosis"@en, "pycnodysostose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XZRTHT6F-V
  skos:prefLabel "fructose intolerance"@en, "intolérance au fructose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-X6PZ6KSL-3
  skos:prefLabel "syndrome cérébrocostomandibulaire"@fr, "cerebrocostomandibular syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CV5K91ZR-G
  skos:prefLabel "Muir-Torre syndrome"@en, "syndrome de Muir-Torre"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XDGV3JXT-H
  skos:prefLabel "tubulopathie héréditaire"@fr, "hereditary tubulopathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QTVB01PR-K
  skos:prefLabel "myopathie némaline"@fr, "nemaline myopathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QT9GTQ4N-0
  skos:prefLabel "ichtyose hystrix"@fr, "ichthyosis hystrix"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GM7NCGPT-9
  skos:prefLabel "hidrotic ectodermal dysplasia"@en, "dysplasie ectodermique hidrotique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JXQ8RQGJ-F
  skos:prefLabel "glossite exfoliatrice marginée"@fr, "geographical tongue"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GJ4RDHFJ-9
  skos:prefLabel "cornea plana"@fr, "cornea plana"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GF8SW923-W
  skos:prefLabel "erythropoietic protoporphyria"@en, "protoporphyrie érythropoïétique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZWPG9CNS-H
  skos:prefLabel "syndrome de Behr"@fr, "Behr syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CQWDC3HQ-X
  skos:prefLabel "MIDAS syndrome"@en, "syndrome de MIDAS"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HJ0D3XSC-S
  skos:prefLabel "déficit en carnitine palmitoyltransférase"@fr, "carnitine O-palmitoyltransferase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JHH6X500-H
  skos:prefLabel "chronic granulomatous disease"@en, "granulomatose septique chronique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CCDM750J-8
  skos:prefLabel "campomelic dysplasia"@en, "nanisme campomélique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JH4LRLKJ-0
  skos:prefLabel "syndrome d'Huriez"@fr, "Huriez syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-X1NTCLP9-2
  skos:prefLabel "acidurie glutarique type 1"@fr, "glutaric aciduria type I"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-K52TXF4H-M
  skos:prefLabel "Hanhart syndrome"@en, "syndrome de Hanhart"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZCRJQ7JS-B
  skos:prefLabel "orocraniodigital syndrome"@en, "syndrome de Juberg Hayward"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-WQHMLFJJ-0
  skos:prefLabel "syndrome de Lowe"@fr, "Lowe syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SQWVFPJK-2
  skos:prefLabel "pseudoxanthoma elasticum"@en, "pseudoxanthome élastique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-W790N3DT-N
  skos:prefLabel "aminoacid disorder"@en, "aminoacidopathie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-G9BHQL64-S
  skos:prefLabel "neurofibromatose de Recklinghausen"@fr, "Recklinghausen's neurofibromatosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JVL4WG1X-L
  skos:prefLabel "protein C deficiency"@en, "déficit en protéine C"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-H2T8C940-R
  skos:prefLabel "dystrophie dermochondrocornéenne"@fr, "dermochondrocorneal dystrophy of François"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QB7RMT32-K
  skos:prefLabel "adenosine deaminase deficiency"@en, "déficit en adénosine désaminase"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-N95H3PMJ-5
  skos:prefLabel "achondroplasia"@en, "achondroplasie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RJ2ZBSVM-H
  skos:prefLabel "anodontie"@fr, "anodontia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CR27D8H3-X
  skos:prefLabel "maladie génétique"@fr, "genetic disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-N32K7HZ8-D .

vh8:-T45BF7ZD-G
  skos:prefLabel "kératodermie palmoplantaire de Thost-Unna"@fr, "Unna-Thost palmoplantar keratoderma"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DVDBBVQP-8
  skos:prefLabel "syndrome de Van Allen-Myhre"@fr, "Van Allen-Myhre syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Q653J5H2-Q
  skos:prefLabel "porokératose de Mibelli"@fr, "Mibelli porokeratosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JC4ZPGWW-B
  skos:prefLabel "Schnyder corneal dystrophy"@en, "dystrophie cornéenne de Schnyder"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GWPN610V-5
  skos:prefLabel "syndrome de Scott"@fr, "Scott syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Z277690J-S
  skos:prefLabel "Christ-Siemens-Touraine syndrome"@en, "syndrome de Christ-Siemens-Touraine"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JG6GHJDH-F
  skos:prefLabel "syndrome d'hyperplasie congénitale de la surrénale"@fr, "congenital adrenal hyperplasia syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BC56H2HC-P
  skos:prefLabel "spondylocostal dysostosis"@en, "dysostose spondylocostale"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QV88W309-T
  skos:prefLabel "Gardner syndrome"@en, "syndrome de Gardner"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RVZ3P800-W
  skos:prefLabel "syndrome de Lesh et Nyhan"@fr, "Lesch-Nyhan syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Z3BPTXLF-D
  skos:prefLabel "syndrome de May-Hegglin"@fr, "May-Hegglin anomaly"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QLJFKDL6-9
  skos:prefLabel "hypochondroplasie"@fr, "hypochondroplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KFMBC1PX-2
  skos:prefLabel "maladie de Darier"@fr, "Darier disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-S18P65KH-F
  skos:prefLabel "kératose folliculaire spinulosique décalvante de Siemens"@fr, "Siemens ichthyosis bullosa"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HQ5GX46Z-X
  skos:prefLabel "syndrome de Stickler"@fr, "Stickler syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-N1KTD1PV-S
  skos:prefLabel "hétéroplasie osseuse progressive"@fr, "progressive osseous heteroplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GR5FH5ZZ-7
  skos:prefLabel "dégénérescence hyaloïdorétinienne de Goldmann et Favre"@fr, "Goldmann-Favre vitroretinal degeneration"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZXDHHJBR-6
  skos:prefLabel "lipofuscinose"@fr, "lipofuscinosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZK7F993P-4
  skos:prefLabel "porokératose actinique"@fr, "actinic porokeratosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-P334XDL2-J
  skos:prefLabel "ichtyose vulgaire"@fr, "ichthyosis vulgaris"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-K7S5JQ62-3
  skos:prefLabel "acropathie ulcéromutilante héréditaire de Thévenard"@fr, "Thevenard hereditary acrodystrophic neuropathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Z2B6G9GP-W
  skos:prefLabel "acidémie isovalérique"@fr, "isovaleric acidemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-W8K8J6P8-3
  skos:prefLabel "Fanconi anemia"@en, "anémie de Fanconi"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KN1MVJP1-7
  skos:prefLabel "syndrome de Keutel"@fr, "Keutel syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XH4T4TXW-2
  skos:prefLabel "Osler-Rendu disease"@en, "angiomatose de Rendu-Osler"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NJGR5JGK-1
  skos:prefLabel "rétinopathie ponctuée albescente"@fr, "retinitis punctata albescens"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-FNQPCVKH-R
  skos:prefLabel "syndrome de Werner"@fr, "Werner syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-S6VW9FXT-P
  skos:prefLabel "syndrome de Simpson-Golabi-Behmel"@fr, "Simpson-Golabi-Behmel syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JHD0JQ5Q-T
  skos:prefLabel "craniodiaphyseal dysplasia"@en, "dysplasie craniodiaphysaire"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CX829SPQ-C
  skos:prefLabel "Barth syndrome"@en, "syndrome de Barth"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZQTHM36F-K
  skos:prefLabel "dysplasie hématodiaphysaire de Ghosal"@fr, "diaphyseal dysplasia with anemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TKPTT4NP-M
  skos:prefLabel "syndrome d'Allgrove"@fr, "Allgrove syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HTTHXG7P-C
  skos:prefLabel "anémie sphérocytaire"@fr, "spherocytic anemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DTGT58D2-K
  skos:prefLabel "dysplasie chondroectodermique"@fr, "chondroectodermal dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XT342XNG-R
  skos:prefLabel "hereditary nonpolyposis colorectal cancer"@en, "cancer colorectal héréditaire non polyposique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TRJ1SD09-W
  skos:prefLabel "Leigh disease"@en, "encéphalomyélopathie nécrosante subaiguë"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-VRW6TJKT-W
  skos:prefLabel "Crouzon disease"@en, "dysostose crâniofaciale de Crouzon"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-D7J8KX7R-Q
  skos:prefLabel "brachyolmie"@fr, "brachyolmia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-D4VR1G17-D
  skos:prefLabel "Klippel-Feil syndrome"@en, "syndrome de Klippel-Feil"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-F9VTM7K5-T
  skos:prefLabel "dysplasie diaphysaire progressive"@fr, "progressive diaphyseal dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-B2GCPK9C-8
  skos:prefLabel "nanisme métatropique"@fr, "metatropic dwarfism"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-C83NFMMK-S
  skos:prefLabel "dégénérescence choriorétinienne héréditaire de la Léventine"@fr, "Leventine chorioretinal degeneration"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CQBS1P5B-7
  skos:prefLabel "syndrome de Kostmann"@fr, "Kostmann syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KF3BT8JV-H
  skos:prefLabel "popliteal pterygium syndrome"@en, "syndrome des ptérygions poplités"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XVNKP097-D
  skos:prefLabel "syndrome de Hennekam"@fr, "Hennekam syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HLG1B0Z1-X
  skos:prefLabel "syndrome d'Hallermann-Streiff-François"@fr, "Hallermann-Streiff-François syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TBFG377G-X
  skos:prefLabel "Huntington disease"@en, "chorée de Huntington"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RPTCZ103-Z
  skos:prefLabel "syndrome de Bartsocas Papas"@fr, "Bartsocas-Papas syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-K7VT1XWZ-R
  skos:prefLabel "Kabuki syndrome"@en, "syndrome Kabuki"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-M0N4TKT5-W
  skos:prefLabel "dysautonomie familiale"@fr, "familial dysautonomia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-T6WMQ6XX-B
  skos:prefLabel "syndrome d'Alport"@fr, "Alport syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QBC2HGP5-9
  skos:prefLabel "dystrophie cornéenne de Groenouw type II"@fr, "Groenouw type II corneal dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-G5MZL975-B
  skos:prefLabel "atrophia gyrata"@fr, "atrophia gyrata"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-D48QVGJZ-0
  skos:prefLabel "fructosemia"@en, "fructosémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-H3GFR5RJ-9
  skos:prefLabel "syndrome de Bazex-Dupré et Christol"@fr, "Bazex-Dupré-Christol syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GZT00M67-Z
  skos:prefLabel "syndrome de Jervell et Lange-Nielsen"@fr, "Jervell and Lange-Nielsen syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DBTWL329-M
  skos:prefLabel "LADD syndrome"@en, "syndrome LADD"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GX96ZXV2-2
  skos:prefLabel "dysgénésie tubulaire rénale"@fr, "renal tubular dysgenesis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-LHRLMTG3-J
  skos:prefLabel "Meleda disease"@en, "kératodermie palmoplantaire de Méléda"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PTSX3DN0-2
  skos:prefLabel "vitréorétinopathie proliférante"@fr, "proliferative vitreoretinopathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RR65K06J-2
  skos:prefLabel "stéatocystomatose multiple"@fr, "steatocystoma multiplex"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-F42NJZ40-Z
  skos:prefLabel "dystrophie cornéenne de Reis-Buckler"@fr, "Reis-Buckler corneal dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GPZR4BFS-X
  skos:prefLabel "dégénérescence en rayon de miel de Doyne"@fr, "Doyne honeycomb retinal degeneration"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-LBB5Q6C9-R
  skos:prefLabel "syndrome de Nezelof"@fr, "Nezelof syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZFX15Q0F-G
  skos:prefLabel "syndrome de Larsen"@fr, "Larsen syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-X9VP93T2-D
  skos:prefLabel "Pelger-Huet anomaly"@en, "anomalie de Pelger-Huet"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-J7MPXHB1-Z
  skos:prefLabel "syndrome de Brugada"@fr, "Brugada syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZP4Q2ST6-8
  skos:prefLabel "syndrome du bébé Michelin"@fr, "Michelin tire baby syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Z8TNPKTB-2
  skos:prefLabel "ictère héréditaire de Crigler et Najjar"@fr, "Crigler-Najjar disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-R5P5V29B-C
  skos:prefLabel "spinocerebellar heredodegeneration"@en, "hérédodégénérescence spinocérébelleuse"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-VXSP9WQJ-7
  skos:prefLabel "dysplasie rétinienne"@fr, "retinal dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-W7B3GJ02-T
  skos:prefLabel "non-bullous ichtyosiform erythroderma"@en, "érythrodermie ichtyosiforme non bulleuse"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CF4BP8DP-G
  skos:prefLabel "renal coloboma syndrome"@en, "syndrome rein-colobome"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MWJQS8SL-Z
  skos:prefLabel "Glanzmann thrombasthenia"@en, "thrombasthénie de Glanzmann"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PFH90FG8-8
  skos:prefLabel "syndrome d'Angelman"@fr, "Angelman syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-WWVN4096-B
  skos:prefLabel "Wolman disease"@en, "maladie de Wolman"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-FRHTZJFN-6
  skos:prefLabel "symphalangie"@fr, "symphalangism"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GFV9Z0SW-R
  skos:prefLabel "dysplasie ectodermique"@fr, "ectodermal dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-FP8QQPSH-1
  skos:prefLabel "rétinopathie pigmentaire"@fr, "pigmentary retinopathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-VZWLPPRV-W
  skos:prefLabel "lymphocytophtisie de Glanzmann"@fr, "Glanzmann-Riniker syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-R5S69L9R-M
  skos:prefLabel "ostéopétrose"@fr, "osteopetrosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XWQ6GL32-W
  skos:prefLabel "Saldino-Noonan syndrome"@en, "syndrome de Saldino-Noonan"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-WQSD96RM-H
  skos:prefLabel "thalassemia"@en, "thalassémie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MG9TNC4F-Q
  skos:prefLabel "dystrophie maculaire annulaire concentrique bénigne"@fr, "benign concentric annular macular dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HKHNT5BS-P
  skos:prefLabel "glycogenosis"@en, "glycogénose"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JL5T2HJT-9
  skos:prefLabel "Weill-Marchesani syndrome"@en, "syndrome de Weill-Marchesani"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-J1Z30DNL-R
  skos:prefLabel "syndrome de Currarino"@fr, "Currarino syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-VHSZS195-R
  skos:prefLabel "cerebrotendinous xanthomatosis"@en, "xanthomatose cérébrotendineuse"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MNZF53TT-J
  skos:prefLabel "kératodermie palmoplantaire striée"@fr, "striate palmoplantar keratoderma"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RD0N82HM-J
  skos:prefLabel "dyschondrostéose"@fr, "dyschondrosteosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NNQK6Q6W-G
  skos:prefLabel "érythrokératodermie variable"@fr, "erythrokeratoderma variabilis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-WK6210CD-T
  skos:prefLabel "Menkes syndrome"@en, "syndrome de Menkes"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NS40662M-D
  skos:prefLabel "ulnar mammary syndrome"@en, "syndrome cubitomammaire"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NFWCC1N5-Q
  skos:prefLabel "syndrome de Pfeiffer"@fr, "Pfeiffer syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JNB3KF12-G
  skos:prefLabel "blue rubber bleb naevus"@en, "syndrome de Bean"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QZGXZRM9-2
  skos:prefLabel "mucoviscidose"@fr, "cystic fibrosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GRQJ2NXX-N
  skos:prefLabel "dermoarthrite histiocytaire familiale"@fr, "familial histiocytic dermatoarthritis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZLVS4FGJ-R
  skos:prefLabel "Stargardt chorioretinal degeneration"@en, "dégénérescence choriorétinienne héréditaire de Stargardt"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TDNL9X15-P
  skos:prefLabel "syndrome de Rapp-Hodgkin"@fr, "Rapp-Hodgkin syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-N5XDC60G-5
  skos:prefLabel "acrocéphalosyndactylie"@fr, "acrocephalosyndactylia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-C7VVC7BW-N
  skos:prefLabel "choroïdérémie"@fr, "choroideremia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JTSMWJJB-7
  skos:prefLabel "ataxie spinocérébelleuse"@fr, "spinocerebellar ataxia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CW64S69F-2
  skos:prefLabel "dégénérescence maculaire pseudoinflammatoire de Sorsby"@fr, "Sorsby macular degeneration"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-M62V5ZC2-F
  skos:prefLabel "hereditary elliptocytosis"@en, "anémie elliptocytaire"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-P9Q0F9M2-F
  skos:prefLabel "syndrome de Pitt-Rogers-Danks"@fr, "Pitt-Rogers-Danks syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MV6JS6DZ-T
  skos:prefLabel "nanisme mésomélique"@fr, "mesomelic dwarfism"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-VSN2N43D-R
  skos:prefLabel "syndrome de Bloom"@fr, "Bloom syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-K17D2MN5-2
  skos:prefLabel "synostose multiple"@fr, "multiple synostosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GJHJZGMJ-H
  skos:prefLabel "syndrome de Carvajal"@fr, "Carvajal syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-L642B2PF-3
  skos:prefLabel "pancréatite chronique familiale"@fr, "hereditary chronic pancreatitis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RT94LQHJ-1
  skos:prefLabel "dyssynergie cérébelleuse myoclonique"@fr, "dyssynergia cerebellia myoclonica"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PV3JPGZL-Q
  skos:prefLabel "Blackfan-Diamond disease"@en, "anémie hypoplasique de Blackfan-Diamond"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CZ8P4KQX-K
  skos:prefLabel "Hailey-Hailey disease"@en, "pemphigus chronique bénin familial"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XZ07C46K-C
  skos:prefLabel "fibromatose juvénile"@fr, "juvenile fibromatosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SKNDPF65-C
  skos:prefLabel "Fuchs corneal dystrophy"@en, "dystrophie endo-épithéliale de Fuchs"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-X4VG7PC6-6
  skos:prefLabel "progressive erythrokeratoderma"@en, "érythrokératodermie progressive"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HMBMF79B-M
  skos:prefLabel "anémie mégaloblastique d'Imerslund"@fr, "Imerslund disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-N3TGF2N9-V
  skos:prefLabel "ichthyosis linearis circumflexa"@en, "ichtyose linéaire circonflexe"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DSV7960J-H
  skos:prefLabel "déficit en acyl-CoA déshydrogénase"@fr, "acyl-CoA dehydrogenase deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-H1M3H8ZH-Q
  skos:prefLabel "frontometaphyseal dysplasia"@en, "dysplasie frontométaphysaire"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GX8GZ9N5-M
  skos:prefLabel "dégénérescence choriorétinienne maculaire de Darris et Coppez"@fr, "Darris-Coppez macular chorioretinal degeneration"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZN8MGQFL-6
  skos:prefLabel "Lin-Gettig syndrome"@en, "syndrome de Lin-Gettig"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-D6XMQL01-N
  skos:prefLabel "desmostérolose"@fr, "desmosterolosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZWPVBTF0-1
  skos:prefLabel "syndrome de Rombo"@fr, "Rombo syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-B75HKZZG-F
  skos:prefLabel "ostéoonychodysostose"@fr, "nail patella syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DRV5RGX9-R
  skos:prefLabel "polyadénomatose endocrinienne de type III"@fr, "multiple endocrine neoplasia type III"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-LCGB1PF6-2
  skos:prefLabel "multiple cartilaginous exostosis"@en, "maladie des exostoses multiples"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XG4MLTB9-J
  skos:prefLabel "syndrome de Muckle et Wells"@fr, "Muckle-Wells syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-K5MR1S4D-Z
  skos:prefLabel "dysplasie spondyloépiphysaire"@fr, "spondyloepiphyseal dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MTJ4WC97-3
  skos:prefLabel "mitochondrial disease"@en, "cytopathie mitochondriale"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-X41QB0LX-K
  skos:prefLabel "foetus arlequin"@fr, "harlequin fetus"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZZD1C200-G
  skos:prefLabel "syndrome de Joubert"@fr, "Joubert syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SL15DT0X-7
  skos:prefLabel "hemophilia"@en, "hémophilie"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KJJT05TH-D
  skos:prefLabel "desquamation familiale continue"@fr, "peeling skin syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Z1VGJVHN-6
  skos:prefLabel "hyperlipoprotéinémie essentielle"@fr, "essential hyperlipoproteinemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XQ46WQ16-B
  skos:prefLabel "syndrome ATR-X"@fr, "ATR-X syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-B9TWB15L-V
  skos:prefLabel "hyperkératose lenticulaire persistante"@fr, "hyperkeratosis lenticularis perstans"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-K20GGS3P-0
  skos:prefLabel "achondrogenesis"@en, "achondrogénèse"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-M38WFJ45-V
  skos:prefLabel "kératodermie palmoplantaire de Vohwinkel"@fr, "Vohwinkel syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BBM4PRQT-B
  skos:prefLabel "WHIM syndrome"@en, "syndrome WHIM"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-TTMRPWR0-Q
  skos:prefLabel "omodysplasie"@fr, "omodysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HF3P255K-H
  skos:prefLabel "syndrome d'hyperimmunoglobulinémie E"@fr, "hyperimmunoglobulinemia E syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PSXV65MW-6
  skos:prefLabel "Wolcott-Rallison syndrome"@en, "syndrome de Wolcott-Rallison"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XDQ7FV5D-L
  skos:prefLabel "Birt-Hogg-Dubé syndrome"@en, "syndrome de Birt-Hogg-Dubé"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-V14901J6-2
  skos:prefLabel "neuropathie tomaculaire"@fr, "tomaculous neuropathy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-N2M310PZ-W
  skos:prefLabel "dysplasie épiphysaire hémimélique"@fr, "dysplasia epiphysialis hemimelica"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SV79FDHT-5
  skos:prefLabel "ostéodysplasie de Melnick-Needles"@fr, "Melnick-Needles osteodysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-B3BK074Z-V
  skos:prefLabel "maladie de Wilson"@fr, "Wilson disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-J269W40Z-H
  skos:prefLabel "chondrodysplasie acromésomélique"@fr, "acromesomelic chondrodysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-FKN242QL-T
  skos:prefLabel "cholostase intrahépatique héréditaire de Summerskill"@fr, "Summerskill disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KJ9T4V22-Q
  skos:prefLabel "hereditary spastic paraplegia"@en, "paraplégie spasmodique héréditaire de Strümpell-Lorrain"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-W1LMNLHN-2
  skos:prefLabel "distichiasis"@fr, "distichiasis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-WN2FQ7Q3-5
  skos:prefLabel "Rothmund-Thomson syndrome"@en, "syndrome de Rothmund-Thomson"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KR00WQ46-J
  skos:prefLabel "cholostase intrahépatique héréditaire de Tygstrup"@fr, "Tygstrup disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-W9GR1T8Z-Q
  skos:prefLabel "dysplasie craniométaphysaire"@fr, "craniometaphyseal dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PZRZP92R-P
  skos:prefLabel "syndrome d'Aicardi"@fr, "Aicardi syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-LLM7LN8S-W
  skos:prefLabel "néphrosialidose"@fr, "nephrosialidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SBKF1MC3-7
  skos:prefLabel "dysplasie artériohépatique"@fr, "arteriohepatic dysplasia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XQD1VXL1-4
  skos:prefLabel "polypose rectocolique familiale"@fr, "familial adenomatous polyposis coli"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-M8W0T5JK-9
  skos:prefLabel "mucolipidose"@fr, "mucolipidosis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HS90PV3R-J
  skos:prefLabel "dégénérescence rétinienne en bave d'escargot"@fr, "snail track retinal degeneration"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-R1JPP52M-8
  skos:prefLabel "microlithiase alvéolaire pulmonaire"@fr, "pulmonary alveolar microlithiasis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-LF9N3HBV-S
  skos:prefLabel "moniléthrix"@fr, "monilethrix"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-GGHSK0G4-8
  skos:prefLabel "anémie dysérythropoïétique congénitale"@fr, "congenital dyserythropoietic anemia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RJW9T491-2
  skos:prefLabel "polyendocrinopathie autoimmune type 1"@fr, "APECED syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-N5WN3GNF-S
  skos:prefLabel "syndrome d'Omenn"@fr, "Omenn syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HKGCMTHZ-W
  skos:prefLabel "Dejerine-Sottas neuropathy"@en, "névrite hypertrophique de Dejerine-Sottas"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-R8Q90Z0M-K
  skos:prefLabel "syndrome de Peutz-Jeghers"@fr, "Peutz-Jeghers syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KN9CVK4Z-N
  skos:prefLabel "Schöpf-Schulz-Passarge syndrome"@en, "syndrome de Schöpf-Schulz-Passarge"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JBD14MNL-G
  skos:prefLabel "hypophosphatemic rickets"@en, "rachitisme hypophosphatémique"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QD9ZH73G-M
  skos:prefLabel "Bruton's agammaglobulinemia"@en, "agammaglobulinémie de Bruton"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KP5HLW1D-9
  skos:prefLabel "dystrophie cornéenne gélatineuse en goutte"@fr, "gelatinous drop-like corneal dystrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-P7496B13-S
  skos:prefLabel "sickle cell anemia"@en, "anémie à hématies falciformes"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-RRMB4HWN-T
  skos:prefLabel "atrophie dentatorubropallidoluysienne"@fr, "dentatorubropallidoluysian atrophy"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-DVC9HSRR-7
  skos:prefLabel "pachyonychie de Jackson-Lawler"@fr, "Jackson-Lawler pachyonychia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-C2L49H54-K
  skos:prefLabel "fructosurie"@fr, "fructosuria"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-NLJ9SXMF-5
  skos:prefLabel "maladie de Refsum"@fr, "Refsum disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BZTPCQN7-B
  skos:prefLabel "syndrome de Coffin-Lowry"@fr, "Coffin-Lowry syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CVM0W1X9-M
  skos:prefLabel "maladie de von Willebrand"@fr, "von Willebrand disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-Z5DZXH85-7
  skos:prefLabel "syndrome de Cockayne"@fr, "Cockayne syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KVW1ZTSK-3
  skos:prefLabel "gérodermie ostéodysplasique"@fr, "osteodysplastic gerodermia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-QSC6VGW6-8
  skos:prefLabel "loose anagen hair syndrome"@en, "syndrome du cheveu anagène caduc"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-VBXFRXMW-4
  skos:prefLabel "paramyotonie congénitale"@fr, "congenital paramyotonia"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-VBF7D9B9-9
  skos:prefLabel "lepréchaunisme"@fr, "leprechaunism"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BFBZPS8B-W
  skos:prefLabel "syndrome lymphoprolifératif autoimmun"@fr, "autoimmune lymphoproliferative syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JNP3VNPD-S
  skos:prefLabel "acrokératose verruciforme de Hopf"@fr, "acrokeratosis verruciformis"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BR640GJ1-S
  skos:prefLabel "dysplasie olfactogénitale"@fr, "Kallmann syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-V5K9J0X9-P
  skos:prefLabel "syndrome de Marfan"@fr, "Marfan syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-ZZBM5ZLH-8
  skos:prefLabel "Kindler syndrome"@en, "syndrome de Kindler"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-MJMJNMFR-1
  skos:prefLabel "severe combined immunodeficiency"@en, "immunodéficit combiné sévère"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-L6N8134K-9
  skos:prefLabel "glucose-6-phosphate dehydrogenase deficiency"@en, "déficit en glucose-6-phosphate déshydrogénase"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-J0B3L2K5-M
  skos:prefLabel "dérèglement immunitaire, polyendocrinopathie, entéropathie, liés à l'X"@fr, "immunodysregulation, polyendocrinopathy, enteropathy, X linked syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-CF6528NT-R
  skos:prefLabel "syndrome de Wiskott-Aldrich"@fr, "Wiskott-Aldrich syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-BVT3K702-Q
  skos:prefLabel "syndrome CINCA"@fr, "CINCA syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-XQ683CNX-W
  skos:prefLabel "cholostase intrahépatique héréditaire de Byler"@fr, "Byler disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-HHHKG0B9-B
  skos:prefLabel "Bernard-Soulier syndrome"@en, "dystrophie thrombocytaire hémorragipare"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-SPKJ93WT-3
  skos:prefLabel "Pendred syndrome"@en, "syndrome de Pendred"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-PJQHTX8P-6
  skos:prefLabel "acrodermatitis enteropathica"@fr, "acrodermatitis enteropática"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-JDT0QQQF-H
  skos:prefLabel "Best macular degeneration"@en, "dégénérescence maculaire de Best"@fr ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .

vh8:-KHS10THT-8
  skos:prefLabel "parkinsonisme familial et fatal avec athymhormie et hypoventilation"@fr, "familial parkinsonian syndrome with athymhormia and hypoventilation"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D .