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Atteintes neurodégénératives, Maladies neurodégénératives, Maladies neurodégénératives de la moelle épinière, Maladies neurodégénératives du SNC, Maladies neurodégénératives du système nerveux central, Troubles neurodégénératifsDegenerative Diseases, Central Nervous System, Degenerative Diseases, Nervous System, Degenerative Diseases, Neurologic, Degenerative Diseases, Spinal Cord, Degenerative Neurologic Diseases, Degenerative Neurologic Disorders, Nervous System Degenerative Diseases, Neurodegenerative Diseases, Neurodegenerative Disorders, Neurologic Degenerative Conditions, Neurologic Degenerative Diseases, Neurologic Diseases, Degenerative - Anomalies monogéniques, génopathie, Génopathies, Génopathies monogéniques, Maladie héréditaire, Maladies génétiques congénitales, Maladies héréditaires, Maladies monogéniquesGenetic Diseases, Inborn, Hereditary Disease, Hereditary Diseases, Inborn Genetic Diseases, Single-Gene Defects[Hyper.]

Dégénérescence hépatocérébrale, Dégénérescence hépatolenticulaire, Dégénérescence hépato-lenticulaire, Dégénérescence hépatolenticulaire progressive, Dégénérescence lenticulaire progressive, Forme hépatique de la maladie de Wilson, Maladie de Wilson, Pseudosclérose cérébrale, Syndrome de Westphal-StrümpellCerebral Pseudosclerosis, Hepatic Form of Wilson Disease, Hepatocerebral Degeneration, Hepatolenticular Degeneration, Hepato-Neurologic Wilson Disease, Kinnier-Wilson Disease, Neurohepatic Degeneration, Progressive Lenticular Degeneration, Pseudosclerosis, Westphal-Strumpell Syndrome, Wilson's Disease, Wilson Disease, Wilson Disease, Hepatic Form - Maladie de Menkès, Syndrome de Menkès, Syndrome des cheveux crépus, Syndrome des cheveux en fil de ferCongenital Hypocupremia, Hypocupremia, Congenital, Kinky Hair Disease, Kinky Hair Syndrome, Menkes' Disease, Menkes Disease, Menkes Kinky Hair Syndrome, Menkes Syndrome, Steely Hair Disease, Steely Hair Syndrome - Nanisme progéroïde, Syndrome de Cockayne, Syndrome de Cockayne groupe A, Syndrome de Cockayne groupe B, Syndrome de Cockayne groupe C, Syndrome de Cockayne type 1, Syndrome de Cockayne type 2, Syndrome de Cockayne type 3, Syndrome de Cockayne type A, Syndrome de Cockayne type B, Syndrome de Cockayne type C, Syndrome de Cockayne type I, Syndrome de Cockayne type II, Syndrome de Cockayne type IIICockayne Syndrome, Cockayne Syndrome, Group A, Cockayne Syndrome, Group B, Cockayne Syndrome, Group C, Cockayne Syndrome, Type A, Cockayne Syndrome, Type B, Cockayne Syndrome, Type C, Cockayne Syndrome, Type I, Cockayne Syndrome, Type II, Cockayne Syndrome, Type III, Group A Cockayne Syndrome, Group B Cockayne Syndrome, Group C Cockayne Syndrome, Progeria-Like Syndrome, Type A Cockayne Syndrome, Type B Cockayne Syndrome, Type C Cockayne Syndrome, Type I Cockayne Syndrome, Type II Cockayne Syndrome, Type III Cockayne Syndrome - Neurofibromatose de type 3, Neurofibromatose de type 3 (NF 3), Neurofibromatoses, Neurofibromes multiples, NF3 (Neurofibromatose type 3)Multiple Neurofibromas, Neurofibromatoses, Neurofibromatosis, Neurofibromatosis 3, Neurofibromatosis Syndrome - Maladie d'AlexanderAlexander's Disease, Alexander Disease - Épilepsie myoclonique progressive type Unverricht-Lundborg, Maladie d'Unverricht-Lundborg, Myoclonus baltique, Myoclonus méditerranéen, Syndrome d'Unverricht-LundborgBaltic Myoclonus, Baltic Myoclonus Epilepsy, Lundborg-Unverricht Syndrome, Mediterranean Myoclonic Epilepsy, Unverricht Disease, Unverricht-Lundborg Syndrome - Amyotrophie de Kugelberg-Welander, Amyotrophie de Werdnig-Hoffmann, Amyotrophie spinale de type 1, Amyotrophie spinale de type 2, Amyotrophie spinale de type 3, Amyotrophie spinale de type I, Amyotrophie spinale de type II, Amyotrophie spinale de type III, Amyotrophie spinale infantile type 1, Amyotrophie spinale infantile type 2, Amyotrophie spinale infantile type 3, Amyotrophie spinale intermédiaire, Amyotrophie spinale juvénile, Amyotrophie spinale proximale type 1, Amyotrophies spinales de l'enfant, Amyotrophies spinales infantiles, ASI (Amyotrophie Spinale Infantile), ASI de type 1, ASI de type 2, ASI de type 3, ASI de type I, ASI de type II, ASI de type III, Atrophie musculaire de Kugelberg-Welander, Atrophie musculaire de Werdnig-Hoffmann, Maladie de Kugelberg-Welander, Maladie de Werdnig-HoffmannHMN (Hereditary Motor Neuropathy) Proximal Type I, HMN Proximal Type I, Infantile Spinal Muscular Atrophy, Juvenile Spinal Muscular Atrophy, Kugelberg-Welander Disease, Muscular Atrophy, Spinal, Infantile, Muscular Atrophy, Spinal, Type I, Muscular Atrophy, Spinal, Type II, Muscular Atrophy, Spinal, Type III, Proximal Hereditary Motor Neuropathy Type I, Spinal Muscular Atrophies of Childhood, Spinal Muscular Atrophy, Infantile, Spinal Muscular Atrophy, Juvenile, Spinal Muscular Atrophy, Type I, Spinal Muscular Atrophy, Type II, Spinal Muscular Atrophy, Type III, Spinal Muscular Atrophy Type I, Spinal Muscular Atrophy Type II, Spinal Muscular Atrophy Type III, Type III Spinal Muscular Atrophy, Type II Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Werdnig Hoffman Disease, Werdnig-Hoffmann Disease - Dégénérescence pallidale pigmentaire, Dystrophie neuroaxonale tardive, Dystrophie neuro-axonale tardive, Maladie de Hallervorden-Spatz, Neurodégénérescence associée à la pantothénate kinase, Neurodégénerescence avec accumulation de fer dans le cerveau, Neuroferritinopathie, Syndrome de Hallervorden-SpatzHallervorden-Spatz Disease, Hallervorden-Spatz Syndrome, Pantothenate Kinase-Associated Neurodegeneration, Pigmentary Pallidal Atrophy, Pigmentary Pallidal Degeneration - Déficit complet en HGPRT, Déficit en hypoxanthine guanine phosphoribosyltransférase, Déficit en hypoxanthine-guanine-phosphoribosyl-transférase, Maladie de Lesch-Nyhan, Syndrome de Lesch-NyhanChoreoathetosis Self-Mutilation Hyperuricemia Syndrome, Complete HGPRT Deficiency Disease, Deficiency Disease, Complete HGPRT, Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase, HGPRT Deficiency Disease, Complete, Hypoxanthine-Phosphoribosyl-Transferase Deficiency Disease, Lesch-Nyhan Disease, Lesch-Nyhan Syndrome - Acro-ostéolyse neurogénique, Acropathie ulcéromutilante familiale, Acropathie ulcéro-mutilante familiale, Insensibilité à la douleur avec anhydrose, Maladie de Thévenard, Neuropathie héréditaire sensitive, Neuropathie héréditaire sensitive et autonome de type 1, Neuropathie héréditaire sensitive et autonome de type 2, Neuropathie héréditaire sensitive et autonome de type 4, Neuropathie héréditaire sensitive et autonome de type 5, Neuropathie héréditaire sensitive et autonome de type I, Neuropathie héréditaire sensitive et autonome de type II, Neuropathie héréditaire sensitive et autonome de type IV, Neuropathie héréditaire sensitive et autonome de type V, Neuropathie héréditaire sensorielle et autonome de type 2, Neuropathie héréditaire sensorielle et autonome de type 4, Neuropathie héréditaire sensorielle et autonome de type 5, Neuropathie héréditaire sensorielle et autonome de type II, Neuropathie héréditaire sensorielle et autonome de type IV, Neuropathie héréditaire sensorielle et autonome de type V, Neuropathie radiculaire sensitive héréditaire, Neuropathies héréditaires sensitives et autonomes, Neuropathies héréditaires sensorielles et autonomes, NHSA, NHSA (Neuropathies Héréditaires Sensitives et Autonomes), NHSA de type 1, NHSA de type 2, NHSA de type 4, NHSA de type 5, NHSA de type I, NHSA de type II, NHSA de type IV, NHSA de type VCongenital Insensitivity to Pain with Anhidrosis, Hereditary Sensory and Autonomic Neuropathies, Hereditary Sensory Autonomic Neuropathy, Type 1, Hereditary Sensory Autonomic Neuropathy, Type 2, Hereditary Sensory Autonomic Neuropathy, Type 4, Hereditary Sensory Autonomic Neuropathy, Type 5, Hereditary Sensory Radicular Neuropathy, HSAN, HSAN (Hereditary Sensory Autonomic Neuropathy), HSAN Type I, HSAN Type II, HSAN Type IV, HSAN Type V, HSN Type I, HSN Type II, Insensitivity to Pain with Anhidrosis, Congenital, Neuropathies, Hereditary Sensory and Autonomic, Pain Insensitivity with Anhidrosis, Congenital, Sensory and Autonomic Neuropathies, Hereditary, Sensory Neuropathy, Hereditary - Dystonia musculorum deformans, Dystonie idiopathique familiale, Dystonie lordotique progressive, Dystonie musculaire déformante, Maladie de Ziehen-Oppenheim, Spasme de torsionChildhood Torsion Disease, Dystonia Deformans Musculorum, Dystonia Deformans Progressiva, Dystonia Musculorum Deformans, Idiopathic Torsion Dystonia, Oppenheim-Ziehen Disease, Progressive Torsion Spasm, Torsion Disease of Childhood, Torsion Dystonia - Épilepsie myoclonique progressive de Lafora, Maladie de Lafora, Maladie de Lafora à début tardif, Myoclonie épileptique progressive de LaforaEpilepsy, Progressive Myoclonic, Lafora, Lafora Body Disease, Lafora Body Disease, Late Onset, Lafora-Body Disease, Late Onset, Lafora Disease, Lafora Progressive Myoclonic Epilepsy, Lafora Type Progressive Myoclonic Epilepsy, Late Onset Lafora Body Disease, Progressive Myoclonic Epilepsy, Lafora, Progressive Myoclonic Epilepsy, Lafora Type - Déficit en aspartoacylase, Dégénérescence spongieuse du système nerveux central, Forme familiale de la maladie de Canavan, Forme juvénile de la maladie de Canavan, Forme sporadique de la maladie de Canavan, Maladie de Canavan, Maladie de Canavan de type 1, Maladie de Canavan de type 2, Maladie de Canavan de type 3, Maladie de Canavan de type I, Maladie de Canavan de type II, Maladie de Canavan de type III, Maladie de Canavan juvénile, Maladie de Canavan néonatale, Maladie de Canavan-von BogaërtCanavan Disease, Canavan Disease, Familial Form, Canavan Disease, Infantile, Canavan Disease, Juvenile, Canavan Disease, Neonatal, Canavan Disease, Sporadic Form, Canavan Disease, Type I, Canavan Disease, Type II, Canavan Disease, Type III, Canavan-van Bogaert-Bertrand Disease, Deficiency Disease, Aspartoacylase, Familial Form of Canavan Disease, Infantile Canavan Disease, Juvenile Canavan Disease, Leukodystrophy, Spongiform, Neonatal Canavan Disease, Spongy Degeneration of Infancy, Spongy Disease of Central Nervous System, Spongy Disease of White Matter, Sporadic Form of Canavan Disease, Type I Canavan Disease, Type II Canavan Disease, Type III Canavan Disease - Syndrome de RettAutism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome, Cerebroatrophic Hyperammonemia, Rett's Disorder, Rett's Syndrome, Rett Disorder, Rett Syndrome - Ataxie cérébelleuse à début précoce, Ataxie cérébelleuse à début tardif, Ataxie cérébelleuse de Pierre Marie, Ataxie cérébelleuse précoce, Ataxie cérébelleuse tardive, Ataxies héréditaires, Dégénérescences cérébelleuses primaires, Dégénérescence spinocérébelleuse de Marinesco-Sjögren, Dégénérescence spino-cérébelleuse de Marinesco-Sjögren, Dégénérescences spinocérébelleuses, Dégénérescences spino-cérébelleuses, Dégénérescences spinocérébelleuses familiales, Dégénérescences spino-cérébelleuses familiales, Dégénérescences spinocérébelleuses héréditaires, Dégénérescences spino-cérébelleuses héréditaires, Hérédoataxie cérébelleuse de Pierre Marie, Hérédo-ataxie cérébelleuse de Pierre Marie, Hérédodégénérescence spinocérébelleuse de Marinesco-Sjögren, Hérédo-dégénérescence spinocérébelleuse de Marinesco-Sjögren, Syndrome de Marinesco-SjögrenAtaxias, Hereditary, Cerebellar Ataxia, Early Onset, Cerebellar Ataxia, Late Onset, Cerebellar Degenerations, Primary, Corticostriatal-Spinal Degeneration, Early Onset Cerebellar Ataxia, Familial Spinocerebellar Degenerations, Hereditary Spinocerebellar Degenerations, Inherited Spinocerebellar Degenerations, Late Onset Cerebellar Ataxia, Marie's Cerebellar Ataxia, Marie Cerebellar Ataxia, Marinesco-Sjogren Syndrome, Marinesco-Sjögren syndrome, Spinocerebellar Degeneration, Spinocerebellar Degenerations, Spino Cerebellar Degenerations, Spino-Cerebellar Degenerations, Spinocerebellar Diseases - Chorée chronique progressive de Huntington, Chorée chronique progressive héréditaire de Huntington, Chorée de Huntington, Maladie de Huntington, Maladie de Huntington à début tardif, Maladie de Huntington juvénile, Maladie de Huntington variante akinétique-rigide, Variante akinétique-rigide de la maladie de HuntingtonAkinetic-Rigid Variant of Huntington Disease, Chorea, Chronic Progressive Hereditary (Huntington), Chronic Progressive Hereditary Chorea (Huntington), Huntington's Chorea, Huntington's Disease, Huntington Chorea, Huntington Chronic Progressive Hereditary Chorea, Huntington Disease, Huntington Disease, Akinetic-Rigid Variant, Huntington Disease, Juvenile, Huntington Disease, Juvenile-Onset, Huntington Disease, Late Onset, Juvenile Huntington Disease, Juvenile-Onset Huntington Disease, Late-Onset Huntington Disease, Progressive Chorea, Chronic Hereditary (Huntington), Progressive Chorea, Hereditary, Chronic (Huntington) - Maladie de Thomsen, Myotonie congénitale, Myotonie congénitale de Becker, Myotonie congénitale de Thomsen, Myotonie généralisée, Myotonie généralisée de BeckerBecker Generalized Myotonia, Generalized Myotonia of Becker, Generalized Myotonia of Thomsen, Myotonia, Generalized, Myotonia, Generalized, Becker, Myotonia Congenita, Myotonia Levior, Thomsen's Disease, Thomsen Disease, Thomsens Disease - Céroïde lipofuschinose neuronale, Céroïde lipofuschinose neuronale de l'adulte, Céroïde lipofuschinose neuronale infantile, Céroïde lipofuschinose neuronale infantile tardive, Céroïde lipofuschinose neuronale juvénile, Céroïde lipofuschinoses neuronales, Céroïde lipofuscinose neuronale, Céroïde lipofuscinose neuronale de l'adulte, Céroïde-lipofuscinose neuronale de l'adulte, Céroïde lipofuscinose neuronale infantile, Céroïde-lipofuscinose neuronale infantile, Céroïde lipofuscinose neuronale infantile tardive, Céroïde-lipofuscinose neuronale infantile tardive, Céroïde lipofuscinose neuronale juvénile, Céroïde-lipofuscinose neuronale juvénile, Céroïde-lipofuscinoses neuronales, Céroïdes lipofuschinoses neuronales, Céroïdes lipofuscinoses neuronales, Céroïdes-lipofuscinoses neuronales, CLN (Céroïde lipofuscinose neuronale), CLN1, CLN2, CLN3, CLN4, Lipofuscinoses céroïdes, Maladie de Batten-Mayou, Maladie de Hagberg-Santavuori, Maladie de Jansky-Bielschowsky, Maladie de Kufs, Maladie de Santavuori-Haltia, Maladie de Spielmeyer-VogtAdult Neuronal Ceroid Lipofuscinosis, Batten Disease, Batten-Mayou Disease, Batten-Spielmeyer-Vogt Disease, Ceroid-Lipofuscinosis, Neuronal, Infantile Neuronal Ceroid Lipofuscinosis, Jansky-Bielschowsky Disease, Juvenile Cerebroretinal Degeneration, Juvenile Neuronal Ceroid Lipofuscinosis, Kufs' disease, Kufs Disease, Late-Infantile Neuronal Ceroid Lipofuscinosis, Lipofuscinosis, Neuronal Ceroid, Neuronal Ceroid-Lipofuscinoses, Neuronal Ceroid-Lipofuscinosis, Neuronal Ceroid Lipofuscinosis, Adult, Neuronal Ceroid Lipofuscinosis, Infantile, Neuronal Ceroid Lipofuscinosis, Juvenile, Neuronal Ceroid Lipofuscinosis, Late-Infantile, Santavuori-Haltia Disease, Spielmeyer-Vogt Disease - Acanthocytose chorée, Chorée acanthocytose, Choréoacanthocytose, Choréo-acanthocytose, Neuroacanthocytose, Syndrome de Levine-CritchleyChorea Acanthocytosis Syndrome, Choreoacanthocytosis, Levine-Critchley Syndrome, Neuroacanthocytosis - Epiloïa, épiloïa, EPILOIA (Epilepsy-Low Intelligence-Adenoma sebaceum), Maladie de Bourneville, Phacomatose de Bourneville, Sclérose tubéreuse, Sclérose tubéreuse de Bourneville, STB (Sclérose Tubéreuse de Bourneville)Bourneville's Disease, Bourneville Disease, Epiloia, Phacomatosis, Bourneville, Phakomatosis, Bourneville, Tuberous Sclerosis - Maladie de Déjerine-Sottas, Neuropathie héréditaire motrice et sensitive de type 3, Neuropathie héréditaire motrice et sensitive de type 7, Neuropathie héréditaire motrice et sensitive de type III, Neuropathie héréditaire motrice et sensitive de type VII, Neuropathie héréditaire motrice et sensorielle de type 3, Neuropathie héréditaire motrice et sensorielle de type 7, Neuropathie héréditaire motrice et sensorielle de type III, Neuropathie héréditaire motrice et sensorielle de type VII, Neuropathies héréditaires motrices et sensitives, Neuropathies héréditaires motrices et sensorielles, Neuropathies motrices et sensorielles héréditaires, Neuropathies sensitivomotrices héréditaires, Neuropathies sensitivo-motrices héréditaires, NMSH, NMSH (Neuropathies Motrices et Sensorielles Héréditaires), NMSH de type 3, NMSH de type 7, NMSH de type III, NMSH de type VIIDejerine-Sottas Disease, Hereditary, Type III, Motor and Sensory Neuropathy, Hereditary, Type VII, Motor and Sensory Neuropathy, Hereditary Motor and Sensory Neuropathies, HMSN, HMSN Type III, HMSN Type VII, Neuropathies, Hereditary Motor and Sensory - Atrophie optique héréditaire, Atrophies optiques héréditaires, Optic Atrophy, HereditaryHereditary Optic Atrophy, Optic Atrophies, Hereditary - Encéphalopathie spongiforme subaigüe type Gerstmann-Straussler, Encéphalopathie spongiforme subaiguë type Gerstmann-Straussler, Syndrome de Gerstmann-Sträussler, Syndrome de Gerstmann-Sträussler-ScheinkerGerstmann-Straussler Inherited Spongiform Encephalopathy, Gerstmann-Straussler-Scheinker Disease, Gerstmann-Straussler Syndrome, Inherited Spongiform Encephalopathy, Gerstmann-Straussler - DM1 (Dystrophie Myotonique de type 1), Dystrophie myotonique, Dystrophie myotonique congénitale, Dystrophie myotonique de Steinert, Dystrophie myotonique de type 1, Maladie de Steinert, Myopathie atrophique avec myotonie, Myotonie atrophique de Steinert, Myotonie dystrophiqueCongenital Myotonic Dystrophy, Dystrophia Myotonica, Myotonia Atrophica, Myotonia Dystrophica, Myotonic Dystrophy, Myotonic Dystrophy, Congenital, Steinert's Disease, Steinert Disease - Retard mental lié à l'X, Retard mental lié au chromosome X, X-Linked Mental Retardation Disorders, X-Linked Mental Retardation SyndromesMental Retardation, X-Linked, X-Linked Mental Retardation - Maladie de Gilles de la Tourette, Maladie des tics, Syndrome de Gilles de la Tourette, Syndrome de TouretteCombined Multiple Motor and Vocal Tic Disorder, Combined Vocal and Multiple Motor Tic Disorder, Gilles de la Tourette's Disease, Gilles de la Tourette Syndrome, Multiple Motor and Vocal Tic Disorder, Combined, Tic Disorder, Combined Vocal and Multiple Motor, Tourette's Disease, Tourette's Disorder, Tourette's Syndrome, Tourette Disease, Tourette Disorder, Tourette Syndrome - Amylose finlandaise, Amylose finnoise, Amylose portugaise, Neuropathie amyloïde de type III, Neuropathie amyloïde familiale de type IV, Neuropathie amyloïde familiale de type portugais, Neuropathie amyloïde familiale de type V, Neuropathie amyloïde familiale de type VI, Neuropathies amyloïdes familiales, Neuropathies amyloïdes héréditaires, Polyneuropathie amyloïde de type 3, Polyneuropathie amyloïde de type Iowa, Polyneuropathie amyloïde familiale de type 1, Polyneuropathie amyloïde familiale de type 2, Polyneuropathie amyloïde familiale de type 4, Polyneuropathie amyloïde familiale de type 5, Polyneuropathie amyloïde familiale de type 6, Polyneuropathie amyloïde familiale de type finlandais, Polyneuropathie amyloïde familiale de type finnois, Polyneuropathie amyloïde familiale de type I, Polyneuropathie amyloïde familiale de type II, Polyneuropathie amyloïde familiale de type III, Polyneuropathie amyloïde familiale de type IV, Polyneuropathie amyloïde familiale de type portugais, Polyneuropathie amyloïde familiale de type suisse, Polyneuropathie amyloïde familiale de type V, Polyneuropathie amyloïde familiale de type VI, Polyneuropathies amyloïdes familialesAmyloid Neuropathies, Familial, Amyloid Polyneuropathy, British Type, Amyloid Polyneuropathy, Iowa Type, Amyloid Polyneuropathy, Swiss Type, Appalachian Type Familial Amyloid Polyneuropathy, British Type Amyloid Polyneuropathy, Familial Amyloid Neuropathy, Andrade Type, Familial Amyloid Neuropathy, Finnish Type, Familial Amyloid Neuropathy, Portuguese Type, Familial Amyloid Polyneuropathies, Familial Amyloid Polyneuropathy, Appalachian Type, Familial Amyloid Polyneuropathy, Jewish Type, Familial Amyloid Polyneuropathy, Type I, Familial Amyloid Polyneuropathy, Type II, Familial Amyloid Polyneuropathy, Type III, Familial Amyloid Polyneuropathy, Type IV, Familial Amyloid Polyneuropathy, Type V, Familial Amyloid Polyneuropathy, Type VI, Finnish Type Familial Amyloid Neuropathy, Iowa Type Amyloid Polyneuropathy, Jewish Type Familial Amyloid Polyneuropathy, Polyneuritic Amyloidosis, Portuguese, Portuguese Polyneuritic Amyloidosis, Portuguese Type Familial Amyloid Neuropathy, Swiss Type Amyloid Polyneuropathy, Type I Familial Amyloid Polyneuropathy, Type II Familial Amyloid Polyneuropathy, Type III Familial Amyloid Polyneuropathy, Type IV Familial Amyloid Polyneuropathy, Type V Familial Amyloid Polyneuropathy, Type VI Familial Amyloid Polyneuropathy - Central Nervous System Demyelinating Hereditary Diseases, Central Nervous System Hereditary Demyelinating Diseases, Demyelinating Central Nervous System Diseases, Hereditary, Demyelinating Diseases, Central Nervous System, Hereditary, Hereditary Demyelinating Diseases, Central Nervous System, Maladies démyélinisantes héréditaires du SNC, Maladies démyélinisantes héréditaires du système nerveux centralCentral Nervous System Demyelinating Diseases, Hereditary, Hereditary Central Nervous System Demyelinating Diseases[Spéc.]

C10.574.500  • C16.320.400  • Degenerative Disease, Nervous System, Hereditary (n.) • Degenerative Hereditary Diseases, Nervous System (n.) • Degenerative Hereditary Disorders, Nervous System (n.) • Hereditary-Degenerative Disorders, Nervous System (n.) • Hereditary Diseases, Neurodegenerative (n.) • Hereditary Neurodegenerative Diseases (n.) • Heredodegenerative Disorders, Nervous System (n.) • Maladies dégénératives héréditaires du système nerveux (n.) • Maladies neurodégénératives héréditaires (n.) • Nervous System Degenerative Hereditary Diseases (n.) • Nervous System Diseases, Degenerative, Hereditary (n.) • Nervous System Hereditary Degenerative Diseases (n.) • Neurodegenerative Diseases, Hereditary (n.)



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