@prefix jvr: . @prefix skos: . @prefix mesh: . @prefix owl: . @prefix dc: . @prefix xsd: . jvr:-WWJHCQRB-K skos:prefLabel "surgery (Qualifier)"@en, "chirurgie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-SDXQ5280-F skos:prefLabel "mortality (Qualifier)"@en, "mortalité (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-HPKB70N8-W skos:prefLabel "rehabilitation (Qualifier)"@en, "rééducation et réadaptation (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-VG20R78F-K skos:prefLabel "embryologie (Qualificatif)"@fr, "embryology (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-Z9TSGBXH-4 skos:prefLabel "génétique (Qualificatif)"@fr, "genetics (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-L6C0XPHT-4 skos:prefLabel "métabolisme (Qualificatif)"@fr, "metabolism (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-WQ00QWRG-J skos:prefLabel "physiopathologie (Qualificatif)"@fr, "physiopathology (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-DH7H9MJ2-N skos:prefLabel "anatomopathologie (Qualificatif)"@fr, "pathology (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-MDQBX560-1 skos:prefLabel "radiotherapy (Qualifier)"@en, "radiothérapie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-ZJBZVRWR-8 skos:prefLabel "parasitologie (Qualificatif)"@fr, "parasitology (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-W6T67RP3-2 skos:prefLabel "diagnostic imaging (Qualifier)"@en, "imagerie diagnostique (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-B6C87218-T skos:prefLabel "prévention et contrôle (Qualificatif)"@fr, "prevention & control (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-J5PBHHGZ-S skos:prefLabel "Protéine P0 de la myéline"@fr, "Myelin P0 Protein"@en ; a mesh:Descriptor, skos:Concept ; skos:related jvr:-HJN06C33-8 . jvr:-BQ3W1P91-F skos:prefLabel "thérapie (Qualificatif)"@fr, "therapy (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-KRXG97RR-5 skos:prefLabel "diagnostic (Qualificatif)"@fr, "diagnosis (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-J9Z93VFN-9 skos:prefLabel "enzymology (Qualifier)"@en, "enzymologie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-T1QJHLQ4-J skos:prefLabel "microbiology (Qualifier)"@en, "microbiologie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-S9KC2ZMS-J skos:prefLabel "Early Growth Response Protein 2"@en, "Facteur de transcription EGR-2"@fr ; a mesh:Descriptor, skos:Concept ; skos:related jvr:-HJN06C33-8 . jvr:-KFM33PF8-L skos:prefLabel "médecine vétérinaire (Qualificatif)"@fr, "veterinary (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr: a skos:ConceptScheme . jvr:-BBD0S71C-R skos:prefLabel "induit chimiquement (Qualificatif)"@fr, "chemically induced (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-XVHTZRCG-7 skos:prefLabel "étiologie (Qualificatif)"@fr, "etiology (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-P1X8SCQ6-K skos:prefLabel "virologie (Qualificatif)"@fr, "virology (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-T6JZ48ZV-N skos:prefLabel "complications (Qualifier)"@en, "complications (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-SDPG013V-D skos:prefLabel "psychology (Qualifier)"@en, "psychologie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-W6SQV79N-S skos:prefLabel "classification (Qualifier)"@en, "classification (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-GXVR9QN8-P skos:prefLabel "drug therapy (Qualifier)"@en, "traitement médicamenteux (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-S0CS1X5R-5 skos:prefLabel "immunology (Qualifier)"@en, "immunologie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-CB30NGKB-3 skos:prefLabel "economics (Qualifier)"@en, "économie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-HJN06C33-8 skos:hiddenLabel "Roussy-Levy Disease"@en, "Neuropathie motrice et sensitive héréditaire de type II"@fr, "NMSH de type 1"@fr, "NHMS de type I"@fr, "Hereditary Areflexic Dystasia"@en, "NMSH de type 2"@fr, "Charcot-Marie-Tooth Neuropathy, Type 1A"@en, "HMSN 1A"@en, "Maladie de Charcot-Marie-Tooth de type Ib"@fr, "Maladie de Charcot-Marie-Tooth de type II"@fr, "Neuropathy, Type II Hereditary Motor and Sensory"@en, "HMSN IA"@en, "Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B"@en, "Hereditary Motor and Sensory Neuropathy 1B"@en, "Charcot-Marie-Tooth Disease, Type IA"@en, "Neuropathy, Type I Hereditary Motor and Sensory"@en, "NMSH de type II"@fr, "Hereditary Type I Motor and Sensory Neuropathy"@en, "HMSN1B"@en, "Neuropathie héréditaire motrice et sensitive de type II"@fr, "Maladie de Charcot-Marie-Tooth de type 1b"@fr, "HMSN I"@en, "Forme axonale de la maladie de Charcot-Marie-Tooth"@fr, "Hereditary Motor And Sensory Neuropathy IB"@en, "Hereditary Motor and Sensory-Neuropathy Type II"@en, "Neuropathie héréditaire motrice et sensitive de type I"@fr, "HMSN1A"@en, "Dystasie aréflexique héréditaire"@fr, "NMSH de type I"@fr, "Charcot-Marie-Tooth Neuropathy, Type 1B"@en, "Syndrome de Roussy-Lévy"@fr, "Maladie de Charcot-Marie-Tooth de type Ia"@fr, "Roussy Levy Hereditary Areflexic Dystasia"@en, "Hereditary Motor, and Sensory Neuropathy Type I"@en, "Neuropathie motrice héréditaire distale de type I"@fr, "Charcot-Marie-Tooth Disease, Demyelinating, Type 1A"@en, "Charcot-Marie-Tooth Disease, Type 1B"@en, "Charcot-Marie-Tooth Disease, Type I"@en, "Hereditary Motor and Sensory Neuropathy 1A"@en, "Charcot-Marie-Tooth Disease, Demyelinating, Type 1B"@en, "Neuropathie héréditaire motrice et sensorielle de type I"@fr, "Dystasie aréflexique héréditaire de Roussy et Lévy"@fr, "Neuropathie motrice et sensitive héréditaire de type I"@fr, "Maladie de Charcot-Marie-Tooth de type I"@fr, "Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy"@en, "Forme hypertrophique de la maladie de Charcot-Marie-Tooth"@fr, "Roussy-Levy Hereditary Areflexic Dystasia"@en, "HMSN IB"@en, "Roussy-Levy Syndrome"@en, "Maladie de Charcot-Marie-Tooth de type 1"@fr, "HMSN Type II"@en, "Charcot-Marie-Tooth Disease, Type II"@en, "Maladie de Charcot-Marie-Tooth de type 2"@fr, "HMN Distal Type I"@en, "Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A"@en, "Charcot-Marie-Tooth Disease, Type IB"@en, "Hereditary Motor and Sensory Neuropathy IA"@en, "Neuropathie motrice héréditaire distale de type 1"@fr, "HMSN II"@en, "Neuropathie héréditaire motrice et sensorielle de type II"@fr, "NHMS de type 1"@fr, "Neuropathie héréditaire motrice et sensitive de type 1"@fr, "Maladie de Charcot-Marie-Tooth de type 1a"@fr, "HMSN Type I"@en, "NHMS de type II"@fr, "Charcot-Marie-Tooth Disease, Type 1A"@en, "NHMS de type 2"@fr, "HMSN 1B"@en, "Neuropathie héréditaire motrice et sensitive de type 2"@fr ; mesh:allowableQualifier jvr:-KFM33PF8-L, jvr:-T6JZ48ZV-N, jvr:-SBNWSM1T-R, jvr:-Z9TSGBXH-4, jvr:-XV06LPML-W, jvr:-XVHTZRCG-7, jvr:-J9Z93VFN-9, jvr:-VG20R78F-K, jvr:-WQ00QWRG-J, jvr:-P1X8SCQ6-K, jvr:-W6T67RP3-2, jvr:-B6C87218-T, jvr:-GXVR9QN8-P, jvr:-BT300B3G-Q, jvr:-BBD0S71C-R, jvr:-ZJBZVRWR-8, jvr:-KRXG97RR-5, jvr:-CB30NGKB-3, jvr:-W4X1LN61-R, jvr:-WWJHCQRB-K, jvr:-L6C0XPHT-4, jvr:-SDXQ5280-F, jvr:-MDQBX560-1, jvr:-CSKTXWF5-F, jvr:-DH7H9MJ2-N, jvr:-W6SQV79N-S, jvr:-BQ3W1P91-F, jvr:-T1QJHLQ4-J, jvr:-JVKFK2NX-2, jvr:-SDPG013V-D, jvr:-NHL3D2X0-S, jvr:-HPKB70N8-W, jvr:-RC3PND0F-S, jvr:-S0CS1X5R-5 ; skos:altLabel "Muscular Atrophy, Peroneal"@en, "Amyotrophie de Charcot-Marie-Tooth"@fr, "Peroneal Muscular Atrophy"@en, "Charcot-Marie-Tooth Hereditary Neuropathy"@en, "Maladie de Charcot-Marie"@fr, "Atrophie musculaire péronière"@fr, "Atrophy, Muscular, Peroneal"@en, "Amyotrophie péronière"@fr, "Charcot-Marie Disease"@en, "Charcot-Marie-Tooth Syndrome"@en ; skos:definition "A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)"@en ; skos:related jvr:-J5PBHHGZ-S, jvr:-S9KC2ZMS-J ; owl:sameAs ; a skos:Concept, mesh:Descriptor ; dc:created "1999-11-08"^^xsd:date ; skos:prefLabel "Charcot-Marie-Tooth Disease"@en, "Maladie de Charcot-Marie-Tooth"@fr ; skos:broader jvr:-DWT3Q63S-2 ; skos:inScheme jvr: ; dc:modified "2013-07-08"^^xsd:date ; dc:established "1991-01-01"^^xsd:date . jvr:-DWT3Q63S-2 skos:prefLabel "Neuropathie héréditaire motrice et sensitive"@fr, "Hereditary Sensory and Motor Neuropathy"@en ; a mesh:Descriptor, skos:Concept ; skos:narrower jvr:-HJN06C33-8 . jvr:-CSKTXWF5-F skos:prefLabel "epidemiology (Qualifier)"@en, "épidémiologie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-BT300B3G-Q skos:prefLabel "cerebrospinal fluid (Qualifier)"@en, "liquide cérébrospinal (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-JVKFK2NX-2 skos:prefLabel "nursing (Qualifier)"@en, "soins infirmiers (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-W4X1LN61-R skos:prefLabel "diet therapy (Qualifier)"@en, "diétothérapie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-RC3PND0F-S skos:prefLabel "ethnology (Qualifier)"@en, "ethnologie (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-XV06LPML-W skos:prefLabel "urine (Qualifier)"@en, "urine (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept . jvr:-NHL3D2X0-S skos:prefLabel "sang (Qualificatif)"@fr, "blood (Qualifier)"@en ; a mesh:Qualifier, skos:Concept . jvr:-SBNWSM1T-R skos:prefLabel "history (Qualifier)"@en, "histoire (Qualificatif)"@fr ; a mesh:Qualifier, skos:Concept .