Informaţii despre

Nume Dystonia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Dystonia, unspecified
Clasificare anatomică Malacards Boli ale urechii; Boli musculare; Boli neuronale
Boli din aceeaşi familie Dystonia 12; Dystonia 16; Dystonia 21; Dystonia 23; Dystonia 24; Dystonia 25; Dystonia 27; Dystonia 9; Dystonia, Juvenile-Onset; Hereditary Dystonia

Vezi şi

Boli A-Z 18p Deletion Syndrome 2-Hydroxyglutaric Aciduria 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome Aceruloplasminemia Achalasia Achalasia-Addisonianism-Alacrima Syndrome Acute Cervicitis Adolescent-Onset Dystonia of Mixed Type Adrenoleukodystrophy Adrenomyodystrophy Agammaglobulinemia Aging Aids Dementia Complex Alcohol Dependence Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alternating Hemiplegia of Childhood Alzheimer Disease 3 Aminoacylase 1 Deficiency Amyotrophic Lateral Sclerosis 2, Juvenile Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Angioedema Aniridia 1 Anorexia Nervosa 1 Anoxia Anterior Cerebral Artery Infarction Anterior Horn Cell Disease Apraxia Apraxia of Eyelid Opening Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Ataxia with Vitamin E Deficiency Athetosis Atlantoaxial Subluxation Attention Deficit-Hyperactivity Disorder Autoimmune Encephalitis Autonomic Neuropathy Basal Ganglia Calcification Basal Ganglia Disease Behr Syndrome Berardinelli-Seip Congenital Lipodystrophy Bipolar I Disorder Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Fracture Borna Disease Brain Injury Branchiootic Syndrome 1 Breast Cancer Bruxism Calcinosis Cardiac Conduction Defect Carpal Tunnel Syndrome Cat Eye Syndrome Causalgia Celiac Disease 1 Central Pontine Myelinolysis Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorinural Hearing Loss Cerebellar Ataxia, Cayman Type Cerebellar Atrophy, Developmental Delay, and Seizures Cerebellar Degeneration Cerebellar Hypoplasia Cerebellopontine Angle Meningioma Cerebral Hypoxia Cerebral Palsy Cerebritis Cerebrotendinous Xanthomatosis Ceroid Lipofuscinosis, Neuronal, 2 Cervical Dystonia Cervicitis Charcot-Marie-Tooth Neuropathy Type 1 Chondrodysplasia Punctata Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoacanthocytosis Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Choroiditis Chronic Pain Chylomicron Retention Disease Citrullinemia, Classic Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly Cocaine Dependence Cockayne Syndrome Complex Regional Pain Syndrome Cornelia De Lange Syndrome Cortical Blindness Corticobasal Degeneration Costello Syndrome Cranio-Facial Dystonia Creutzfeldt-Jakob Disease Crouzon Syndrome with Acanthosis Nigricans Cyanosis, Transient Neonatal Dementia Dentatorubral-Pallidoluysian Atrophy Diabetes Mellitus Diencephalic Syndrome Diffuse Idiopathic Skeletal Hyperostosis Donnai-Barrow Syndrome Doyne Honeycomb Retinal Dystrophy Drug-Induced Hepatitis Dyschromatosis Symmetrica Hereditaria Dyschromatosis Universalis Hereditaria 3 Dysgraphia Dyskinetic Cerebral Palsy Dysphagia Dystonia 11, Myoclonic Dystonia 12 Dystonia 13, Torsion, Autosomal Dominant Dystonia 15, Myoclonic Dystonia 16 Dystonia 17, Torsion, Autosomal Recessive Dystonia 1, Torsion, Autosomal Dominant Dystonia 21 Dystonia 23 Dystonia 24 Dystonia 27 Dystonia 2, Torsion, Autosomal Recessive Dystonia 3, Torsion, X-Linked Dystonia 4, Torsion, Autosomal Dominant Dystonia 6, Torsion Dystonia 7, Torsion Dystonia, Dopa-Responsive Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency Dystonia, Focal, Task-Specific Dystonia, Juvenile-Onset Dystonia/parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease Dyt1 Early-Onset Isolated Dystonia Early-Onset Generalized Dystonia Early-Onset Generalized Limb-Onset Dystonia Early-Onset Parkinson Disease Encephalitis Encephalomyopathy Encephalopathy Entropion Ependymoma Epilepsy Epileptic Encephalopathy, Early Infantile, 16 Episodic Ataxia Episodic Ataxia, Type 2 Episodic Kinesigenic Dyskinesia 1 Epithelial Recurrent Erosion Dystrophy Erdheim-Chester Disease Essential Tremor Extrapontine Myelinolysis Facioscapulohumeral Muscular Dystrophy 1 Familial Idiopathic Basal Ganglia Calcification Fanconi Anemia, Complementation Group E Fibromatosis Fibrous Histiocytoma Focal Dystonia Focal Epilepsy Focal Hand Dystonia Fontaine Progeroid Syndrome Frontotemporal Dementia Fucosidosis Gastroesophageal Reflux Gilles De La Tourette Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glioma Glucose Transporter Type 1 Deficiency Syndrome Glutaric Acidemia I Glycogen Storage Disease Ii Gm1-Gangliosidosis, Type Iii Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia Hartnup Disorder Headache Hemidystonia Hemifacial Spasm Hemifacial Spasm, Familial Hemiplegia Hemiplegic Migraine Hemoglobinuria Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hereditary Dystonia Hereditary Sensory Neuropathy Hereditary Spastic Paraplegia Histiocytoma Histiocytosis Homocystinuria Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperacusis Hypermanganesemia with Dystonia Hypermanganesemia with Dystonia 1 Hypermobility Syndrome Hyperostosis Hyperphenylalaninemia Hyperphenylalaninemia, Bh4-Deficient, a Hyperphenylalaninemia, Bh4-Deficient, B Hyperreflexia Hypertonia Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoparathyroidism Hypotonia Hypoxia Ichthyosis Idiopathic Scoliosis Impulse Control Disorder Infantile Epileptic Encephalopathy Infantile Hypotonia Inner Ear Disease Ischemia Juvenile Amyotrophic Lateral Sclerosis Kallmann Syndrome Kearns-Sayre Syndrome Langerhans Cell Histiocytosis Laryngitis Laryngomalacia Lateral Medullary Syndrome Lateral Sclerosis Learning Disability Leber Hereditary Optic Neuropathy Leber Optic Atrophy and Dystonia Leigh Syndrome Leukodystrophy Leukodystrophy, Hypomyelinating, 2 Leukodystrophy, Hypomyelinating, 6 Leukomalacia Linear Scleroderma Lingual-Facial-Buccal Dyskinesia Lipodystrophy Lipoid Proteinosis of Urbach and Wiethe Liver Disease Localized Scleroderma Lubs X-Linked Mental Retardation Syndrome Lymphedema, Hereditary, Ii Machado-Joseph Disease Mcleod Syndrome Megaesophagus Melanocytic Nevus Syndrome, Congenital Meningitis Meningoencephalitis Metachromatic Leukodystrophy Methanol Poisoning Microcephaly Mohr-Tranebjaerg Syndrome Molybdenum Cofactor Deficiency Mononeuropathy of the Median Nerve, Mild Mood Disorder Movement Disease Moyamoya Disease 1 Mucolipidosis Iv Multifocal Dystonia Multiple Sclerosis Multiple System Atrophy 1 Muscular Dystrophy Mutism Myasthenia Gravis Myoclonus Myotonia Nephrotic Syndrome Nephrotic Syndrome, Type 1 Neuraminidase Deficiency Neuroaxonal Dystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation Neurodegeneration with Brain Iron Accumulation 1 Neurodegeneration with Brain Iron Accumulation 2a Neurodegeneration with Brain Iron Accumulation 2b Neurodegeneration with Brain Iron Accumulation 3 Neurodegeneration with Brain Iron Accumulation 4 Neurodegeneration with Brain Iron Accumulation 5 Neurodegeneration with Brain Iron Accumulation 6 Neurofibromatosis, Type Iv, of Riccardi Neuroleptic Malignant Syndrome Neuromyelitis Optica Neuronal Intranuclear Inclusion Disease Neuronitis Neuropathy Neurosyphilis Obsessive-Compulsive Disorder Oculogyric Crisis Oligoastrocytoma Opsoclonus-Myoclonus Syndrome Oromandibular Dystonia Osteoporotic Fracture Pachygyria Paine Syndrome Paraplegia Parkinson Disease 14, Autosomal Recessive Parkinson Disease 15, Autosomal Recessive Early-Onset Parkinsonism-Dystonia, Infantile Paroxysmal Choreoathetosis Paroxysmal Nocturnal Hemoglobinuria Pathological Gambling Periodontitis Periventricular Leukomalacia Periventricular Nodular Heterotopia Persistent Vegetative State Pharyngitis Photosensitive Epilepsy Piriformis Syndrome Plexopathy Polycythemia Pontocerebellar Hypoplasia Progressive Multifocal Leukoencephalopathy Pseudobulbar Palsy Pseudohypoparathyroidism Psychogenic Movement Quadriplegia Radiculopathy Reflex Sympathetic Dystrophy Repetitive Motion Disorders Restless Legs Syndrome Rett Syndrome Rheumatic Encephalitis Ring Chromosome 2 Ring Chromosome 21 Sakati Syndrome Sandifer Syndrome Schizencephaly Schizophrenia Schnyder Corneal Dystrophy Scoliosis Segawa Syndrome, Autosomal Recessive Segmental Dystonia Seizures, Benign Familial Neonatal, 1 Serpiginous Choroiditis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Siderosis Silver-Russell Syndrome Sleep Disorder Spasmodic Dysphonia Spasmodic Dystonia Spastic Ataxia Spastic Cerebral Palsy Spasticity Spastic Paraparesis Spinal Cord Ependymoma Spinal Stenosis Spinocerebellar Ataxia 17 Spinocerebellar Ataxia 36 Spinocerebellar Ataxia Type 16 Spinocerebellar Atrophy Spiradenoma Spondyloocular Syndrome Striatonigral Degeneration Sturge-Weber Syndrome Stuttering Subacute Cerebellar Degeneration Succinic Semialdehyde Dehydrogenase Deficiency Superficial Siderosis Supranuclear Palsy, Progressive, 1 Sveinsson Chorioretinal Atrophy Swallowing Disorders Syringomyelia Systemic Mastocytosis Talipes Equinovarus Tardive Dyskinesia Temporal Lobe Epilepsy Tetrahydrobiopterin Deficiency Thiamine Metabolism Dysfunction Syndrome 2 Thoracic Outlet Syndrome Thyroid Cancer, Nonmedullary, 1 Thyroiditis Tic Disorder Torsion Dystonia with Onset in Infancy Torticollis Toxoplasmoză Transient Global Amnesia Traumatic Brain Injury Tremor Tuberculous Meningitis Turner Syndrome Ulnar Neuropathy Vitamin B12 Deficiency Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Weber Syndrome West Syndrome Whipple Disease Wilson Disease Woodhouse-Sakati Syndrome Xanthomatosis X-Linked Dystonia-Parkinsonism/lubag Yemenite Deaf-Blind Hypopigmentation Syndrome