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Nume Ataxia and Polyneuropathy, Adult-Onset
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice
Clasificari ICD10 Ataxia, unspecified

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Boli A-Z 3-Methylglutaconic Aciduria, Type V 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Acanthosis Nigricans Acardia Aceruloplasminemia Achalasia-Addisonianism-Alacrima Syndrome Acute Disseminated Encephalomyelitis Acute Leukemia Acute Liver Failure Acute Motor and Sensory Axonal Neuropathy Acute Motor Axonal Neuropathy Acute Mountain Sickness Adenocarcinoma Adermatoglyphia Adrenoleukodystrophy Agammaglobulinemia Aging Agnosia Albinism Alexander Disease Alexia Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Aminoaciduria Amyloidosis Amyloidosis, Hereditary, Transthyretin-Related Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 Analbuminemia Anauxetic Dysplasia 1 Anemia, Sideroblastic, 1 Anemia, Sideroblastic, and Spinocerebellar Ataxia Aneurysm Angelman Syndrome Angiolipoma Aniridia 1 Anorexia Nervosa 1 Anosmia Anosognosia Anterior Horn Cell Disease Antiphospholipid Syndrome Apraxia Arbitrary Restriction Polymorphism 1 Argyll Robertson Pupil Artemis Deficiency Arteries, Anomalies of Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Deafness-Retardation Syndrome Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia Ataxia-Microcephaly-Cataract Syndrome Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Oculomotor Apraxia 4 Ataxia-Pancytopenia Syndrome Ataxia-Telangiectasia Ataxia with Vitamin E Deficiency Athetosis Aural Atresia, Congenital Autoimmune Disease Autoimmune Encephalitis Autoimmune Polyendocrine Syndrome Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Cerebellar Ataxia Autosomal Recessive Cerebellar Ataxia Autosomal Recessive Disease Autosomal Recessive Sideroblastic Anemia Axonal Neuropathy Babesiosis Back Pain Basal Ganglia Disease B-Cell Lymphomas Bilateral Breast Cancer Biliary Atresia Biotinidase Deficiency Bipolar Disorder Bladder Cancer Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group--Rhesus System E Polypeptide Bloom Syndrome Blue Rubber Bleb Nevus Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Borna Disease Boucher-Neuhauser Syndrome Brain Edema Brain Injury Brainstem Auditory Evoked Responses Branchiootic Syndrome 1 Breast Cancer Bronchopneumonia Brugada Syndrome Burkitt Lymphoma Camurati-Engelmann Disease Cataract Cataract, Ataxia, Short Stature, and Mental Retardation Celiac Disease 1 Central Nervous System Lymphoma Central Nervous System Origin Vertigo Central Pontine Myelinolysis Central Sleep Apnea Cerebellar Ataxia and Neurosensory Deafness Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, and Sensorineural Hearing Loss Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorinural Hearing Loss Cerebellar Ataxia, Cayman Type Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant Cerebellar Ataxia, Early-Onset, with Retained Tendon Reflexes Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome Cerebellar Degeneration Cerebellar Disease Cerebellar Hypoplasia Cerebello-Olivary Atrophy Cerebral Degeneration Cerebral Palsy Cerebritis Cerebrotendinous Xanthomatosis Ceroid Lipofuscinosis, Neuronal, 2 Cervical Cancer Cervical Dystonia Cervicitis Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease, Axonal, Type 2t Chickenpox Chikungunya Childhood Apraxia of Speech Childhood Ataxia with Central Nervous System Hypomyelination/vanishing White Matter Childhood Leukemia Chloramphenicol Toxicity Cholangiocarcinoma Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Chorioretinitis Choroiditis Chromosomal Triplication Chronic Active Epstein-Barr Virus Infection Chronic Eosinophilic Pneumonia Chronic Inflammatory Demyelinating Polyneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Pain Chronic Progressive External Ophthalmoplegia Ciliary Dyskinesia, Primary, 1 Cleft Larynx, Posterior Coach Syndrome Coarctation of Aorta Cockayne Syndrome Cognitive Function 1, Social Coloboma of Iris Colonic Pseudo-Obstruction Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone Dystrophy Congenital Disorder of Glycosylation, Type Ia Congenital Hepatic Fibrosis Congenital Hypothyroidism Congenital Nystagmus Congestive Heart Failure Conjunctivitis Corneal Dystrophy Cortical Blindness Corticobasal Degeneration Cowden Disease Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniopharyngioma Craniosynostosis 1 Creutzfeldt-Jakob Disease Crohn's Colitis Crohn's Disease Cystic Fibrosis Cystinuria Cystitis Dandy-Walker Complex D-Bifunctional Protein Deficiency Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Dementia Demyelinating Polyneuropathy Dengue Virus Dentatorubral-Pallidoluysian Atrophy Dermatitis Dermatitis Herpetiformis De Sanctis-Cacchione Syndrome Developmental Coordination Disorder Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diarrhea Dicarboxylic Aminoaciduria Diffuse Alveolar Hemorrhage Diffuse Large B-Cell Lymphoma Dilated Cardiomyopathy Disseminated Peritoneal Leiomyomatosis Donnai-Barrow Syndrome Down Syndrome Duane Retraction Syndrome 1 Dysautonomia Dyschromatosis Symmetrica Hereditaria Dysphagia Dystonia Early Onset Absence Epilepsy Ectodermal Dysplasia Encephalitis Encephalomyopathy Encephalopathy Endodermal Sinus Tumor Endotheliitis Eosinophilic Pneumonia Ependymoma Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica Epilepsy Epilepsy, Progressive Myoclonic 7 Episodic Ataxia Episodic Ataxia, Type 1 Episodic Ataxia, Type 2 Episodic Ataxia, Type 4 Episodic Ataxia, Type 6 Erdheim-Chester Disease Erythromelalgia Esophageal Cancer Essential Tremor Exencephaly Extrapontine Myelinolysis Familial Hemiplegic Migraine Familial Retinoblastoma Fanconi Anemia, Complementation Group E Fatal Familial Insomnia Fibrous Histiocytoma Fmr1-Related Primary Ovarian Insufficiency Focal Dystonia Focal Epilepsy Foot Drop Form Agnosia Fragile X-Associated Tremor/ataxia Syndrome Fragile X Syndrome Fragile X Tremor/ataxia Syndrome Friedreich Ataxia 1 Friedreich Ataxia 2 Ganglioneuroblastoma Ganglioneuroma Gastric Cancer Gastroparesis Gerstmann-Straussler Disease Gigantism Gillespie Syndrome Glioblastoma Glioblastoma Multiforme Glioma Glucose Transporter Type 1 Deficiency Syndrome Gonadoblastoma Gordon Holmes Syndrome Granulocytopenia Graves' Disease Growth Hormone Deficiency Haemophilus Influenzae Hair Disease Hashimoto's Encephalitis Hashimoto Thyroiditis Headache Hemifacial Atrophy, Progressive Hemiplegia Hemiplegic Migraine Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hemorrhagic Cystitis Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatoblastoma Hepatocellular Carcinoma Hereditary Ataxia Hereditary Sensory Neuropathy Hereditary Spastic Paraplegia Hereditary Wilms' Tumor Herpes Simplex Herpes Zoster Herpes Zoster Ophthalmicus Histiocytoma Histiocytosis Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance Homocystinuria Human Immunodeficiency Virus Type 1 Huntington Disease Hydrocephalus Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 Hydrolethalus Syndrome 1 Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertonia Hypertrophia Musculorum Vera Hypertrophic Cardiomyopathy Hypobetalipoproteinemia, Familial, 1 Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypotonia Hypotonia, Congenital Nystagmus, Ataxia and Abnormal Auditory Brainstem Response Hypotonia, Congenital Nystagmus, Ataxia, and Abnormal Auditory Brainstem Responses Hypoxia Ichthyosis Prematurity Syndrome Immunoglobulin Alpha Deficiency Incontinentia Pigmenti Infertility Inflammatory Bowel Disease Influenza Insulin-Like Growth Factor I Internuclear Ophthalmoplegia Interstitial Lung Disease Intracranial Aneurysm Intracranial Hypotension Ischemia Isoniazid Toxicity Kallmann Syndrome Kearns-Sayre Syndrome Krabbe Disease Kufor-Rakeb Syndrome L-2-Hydroxyglutaric Aciduria Lactic Acidosis Lambert-Eaton Myasthenic Syndrome Langerhans Cell Histiocytosis Laryngeal Abductor Paralysis Laryngitis Lateral Medullary Syndrome Lateral Sclerosis Learning Disability Leber Congenital Amaurosis 4 Leber Hereditary Optic Neuropathy Legionellosis Leigh Syndrome Leiomyoma Leiomyosarcoma Leishmaniasis Leptospirosis Leukemia Leukodystrophy Leukoencephalopathy with Vanishing White Matter Lichtenstein-Knorr Syndrome Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Light Fixation Seizure Syndrome Limbic Encephalitis Lipid Metabolism Disorder Liver Disease Lubs X-Linked Mental Retardation Syndrome Lung Cancer Lung Cancer Susceptibility 1 Lung Disease Lupus Erythematosus Lyme Disease Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoma Lymphoma, Hodgkin, Classic Lymphoma, Mucosa-Associated Lymphoid Type Lymphosarcoma Lysosomal Storage Disease Machado-Joseph Disease Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Majeed Syndrome Malaria Malignant Hyperthermia Malignant Pleural Mesothelioma Mannosidosis Mannosidosis, Alpha B, Lysosomal Mannosidosis, Beta a, Lysosomal Mantle Cell Lymphoma Marchiafava Bignami Disease Marden-Walker Syndrome Marinesco-Sjogren Syndrome Mature Teratoma Megalencephaly Megalencephaly with Dysmyelination Melanoma Meningitis Meningococcal Meningitis Meningoencephalitis Metachromatic Leukodystrophy Mevalonic Aciduria Microcephaly Microcephaly, Epilepsy, and Diabetes Syndrome Middle Ear Cholesterol Granuloma Miller Fisher Syndrome Mirror Agnosia Mitochondrial Complex Iii Deficiency Mitochondrial Disorders Mitochondrial Dna Depletion Syndrome 7 Mitochondrial Encephalomyopathy Mitochondrial Metabolism Disease Mitochondrial Myopathy Mood Disorder Motion Sickness Motor Neuron Disease Mousa Al Din Al Nassar Syndrome Mucocutaneous Leishmaniasis Mucolipidosis Iv Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Vii Mucositis Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple System Atrophy 1 Multiple System Atrophy, Cerebellar Type Mumps Muscular Atrophy Muscular Dystrophy Musical Perfect Pitch Mutagen Sensitivity Myeloid Leukemia Myhre Syndrome Myocardial Infarction Myoclonus Myoclonus and Ataxia Myoclonus Epilepsy Myoepithelioma Myofibrillar Myopathy Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 Myopia Myotonic Dystrophy Myxedema Narcolepsy Necrobiosis Lipoidica Nephronophthisis Nephrotic Syndrome Neural Crest Tumor Neuritis Neuroaxonal Dystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuromuscular Disease Neuronal Ceroid Lipofuscinosis Neuronal Intranuclear Inclusion Disease Neuronitis Neuropathy Neuropathy, Ataxia, and Retinitis Pigmentosa Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neurosarcoidosis Neurosyphilis Nicolaides-Baraitser Syndrome Nijmegen Breakage Syndrome Nodular Regenerative Hyperplasia Nonalcoholic Steatohepatitis Obstructive Hydrocephalus Ocular Motor Apraxia Olivopontocerebellar Atrophy Opsoclonus-Myoclonus Syndrome Optic Atrophy 3, Autosomal Dominant Optic Neuritis Oral Cancer Oromandibular Dystonia Orthostatic Intolerance Osteogenic Sarcoma Otitis Media Ovarian Cancer Ovarian Gonadoblastoma Ovary Papillary Carcinoma Pancreatitis Pancytopenia Papillary Carcinoma Papilloma Papillomatosis, Confluent and Reticulated Paralytic Poliomyelitis Paraneoplastic Cerebellar Degeneration Paraneoplastic Syndromes Paraplegia Paresthesia Parkinson Disease 7, Autosomal Recessive Early-Onset Parkinson Disease Type 9 Pellagra Perilymphatic Fistula Peroxisomal Biogenesis Disorders Perrault Syndrome Persistent Idiopathic Facial Pain Pharyngeal-Cervical-Brachial Variant of Guillain-Barré Syndrome Pharyngitis Pharynx Cancer Pineoblastoma Plasmodium Falciparum Malaria Plasmodium Vivax Malaria Pneumonia Pneumothorax Poliomyelitis Polydactyly Polykaryocytosis Inducer Polyneuropathy Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract Polyradiculoneuropathy Polyradiculopathy Pontine Hemorrhage Pontocerebellar Hypoplasia Posterior Column Ataxia Posterior Column Ataxia with Retinitis Pigmentosa Premature Ovarian Failure 1 Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia Primary Agammaglobulinemia Primary Central Nervous System Lymphoma Primary Cerebellar Degeneration Prion Disease Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Progressive Myoclonus Epilepsy Prolymphocytic Leukemia Prostatitis Pseudohypoparathyroidism Ptosis Pulmonary Tuberculosis Pulmonary Valve Stenosis Purpura Pyruvate Kinase Deficiency of Red Cells Refsum Disease, Classic Rem Sleep Behavior Disorder Restless Legs Syndrome Retinal Degeneration Retinitis Retinitis Pigmentosa Retinoblastoma Retroperitoneal Fibrosis Rhabdomyosarcoma Rhombencephalosynapsis Rosacea Rosai-Dorfman Disease Samd9l-Related Ataxia-Pancytopenia Syndrome Sandhoff Disease Sarcoma Schizophrenia Scn2a Related Disorders Scoliosis Seckel Syndrome Secretory Diarrhea Seizures, Benign Familial Neonatal, 1 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Sensorineural Hearing Loss Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Short Bowel Syndrome Sideroblastic Anemia Siderosis Simultanagnosia Sjogren Syndrome Sleep Apnea Sleep Disorder Small Cell Carcinoma Smith-Kingsmore Syndrome Smith-Mccort Dysplasia 1 Somatization Disorder Spasmodic Dystonia Spastic Ataxia Spastic Ataxia 3, Autosomal Recessive Spastic Ataxia, Charlevoix-Saguenay Type Spastic Diplegia Spasticity Spastic Paraparesis Spastic Paraplegia 20, Autosomal Recessive Spastic Paraplegia 30, Autosomal Recessive Spastic Paraplegia 46, Autosomal Recessive Spastic Paraplegia 7, Autosomal Recessive Speech Disorder Spinal Muscular Atrophy Spinocerebellar Ataxia 1 Spinocerebellar Ataxia 10 Spinocerebellar Ataxia 11 Spinocerebellar Ataxia 12 Spinocerebellar Ataxia 13 Spinocerebellar Ataxia 14 Spinocerebellar Ataxia 15 Spinocerebellar Ataxia 17 Spinocerebellar Ataxia 18 Spinocerebellar Ataxia 19 Spinocerebellar Ataxia 2 Spinocerebellar Ataxia 20 Spinocerebellar Ataxia 21 Spinocerebellar Ataxia 23 Spinocerebellar Ataxia 25 Spinocerebellar Ataxia 26 Spinocerebellar Ataxia 27 Spinocerebellar Ataxia 28 Spinocerebellar Ataxia 29 Spinocerebellar Ataxia 31 Spinocerebellar Ataxia 34 Spinocerebellar Ataxia 35 Spinocerebellar Ataxia 36 Spinocerebellar Ataxia 37 Spinocerebellar Ataxia 38 Spinocerebellar Ataxia 4 Spinocerebellar Ataxia 43 Spinocerebellar Ataxia 5 Spinocerebellar Ataxia 6 Spinocerebellar Ataxia 7 Spinocerebellar Ataxia 8 Spinocerebellar Ataxia, Autosomal Recessive 1 Spinocerebellar Ataxia, Autosomal Recessive 15 Spinocerebellar Ataxia, Autosomal Recessive 20 Spinocerebellar Ataxia, Autosomal Recessive 3 Spinocerebellar Ataxia, Autosomal Recessive 7 Spinocerebellar Ataxia, Autosomal Recessive 8 Spinocerebellar Ataxia Type 16 Spinocerebellar Ataxia Type 19/22 Spinocerebellar Ataxia Type 1 with Axonal Neuropathy Spinocerebellar Ataxia with Axonal Neuropathy Type 2 Spinocerebellar Atrophy Spinocerebellar Degeneration Spontaneous Intracranial Hypotension Sporadic Adult-Onset Ataxia of Unknown Etiology Squamous Cell Carcinoma Steatorrhea Stiff-Person Syndrome Strabismus Subcortical Arteriosclerotic Encephalopathy Superficial Siderosis Superficial Siderosis of the Central Nervous System Swallowing Disorders Swayback Syndrome of Inappropriate Antidiuretic Hormone Syne1-Related Autosomal Recessive Cerebellar Ataxia Syphilitic Myelopathy Systemic Lupus Erythematosus Tabes Dorsalis Tay-Sachs Disease T Cell Deficiency T-Cell Leukemia T-Cell Lymphoma 1a T-Cell Prolymphocytic Leukemia Telangiectasis Temporal Lobe Epilepsy Teratoma Testicular Regression Syndrome Testicular Yolk Sac Tumor Tetraamelia Syndrome, Autosomal Recessive Thrombasthenia Thrombocytopenia Thrombosis Thyroid Cancer, Nonmedullary, 1 Thyroiditis Tic Disorder Tick Paralysis Tooth Disease Torticollis Toxocariasis Traumatic Brain Injury Tremor Trigeminal Neuralgia Tuberous Sclerosis Tularemia Tumor Suppressor Gene on Chromosome 11 Typhoid Fever Tyrosinemia Virus Associated Hemophagocytic Syndrome Visual Agnosia Vitamin B12 Deficiency Vitamin E, Familial Isolated Deficiency of Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Werner Syndrome Wernicke-Korsakoff Syndrome West Nile Virus Whipple Disease Wilms Tumor 6 Woodhouse-Sakati Syndrome Xanthomatosis Xeroderma Pigmentosum, Complementation Group F X-Ray Sensitivity