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Nume Tremor
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Tremor, unspecified
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Essential Tremor; Tremor, Hereditary Essential, 1; Tremor, Hereditary Essential, 2; Tremor, Hereditary Essential, 3; Tremor, Hereditary Essential, 4; Tremor, Hereditary Essential, 5

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Boli A-Z 2-Hydroxyglutaric Aciduria 48,xxyy Syndrome Abetalipoproteinemia Acoustic Neuroma Acquired Immunodeficiency Syndrome Adenocarcinoma Adult Polyglucosan Body Disease Aging Agnosia Alcohol Abuse Alexander Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Methylacyl-Coa Racemase Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloid Neuropathy Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 Androgen Insensitivity Syndrome, Mild Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Anterior Horn Cell Disease Aphasia Apraxia Apraxia of Eyelid Opening Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Athetosis Audiogenic Seizures Autonomic Dysfunction Axonal Neuropathy Basal Ganglia Calcification Behr Syndrome Bell's Palsy Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bobble-Head Doll Syndrome 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 Brain Germinoma Brain Injury Brainstem Auditory Evoked Responses Brain Stem Infarction Branchiootic Syndrome 1 Brucellosis Bruxism Canavan Disease Cavernous Malformation Celiac Disease 1 Central Nervous System Germinoma Central Pontine Myelinolysis Cerebellar Degeneration Cerebellar Disease Cerebellar Hypoplasia Cerebral Atrophy Cerebral Meningioma Cerebritis Cervical Dystonia Cervicitis Charcot-Marie-Tooth Disease Cholera Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Choroiditis Chromosomal Triplication Chronic Inflammatory Demyelinating Polyneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chylomicron Retention Disease Citrullinemia, Classic Cone-Rod Dystrophy 2 Conversion Disorder Corticobasal Degeneration Craniosynostosis 1 Crouzon Syndrome with Acanthosis Nigricans Cytochrome P450 2d6 Variant Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Dementia Dementia, Lewy Body Demyelinating Polyneuropathy Dentatorubral-Pallidoluysian Atrophy Donnai-Barrow Syndrome Duodenal Obstruction Duodenitis Dysautonomia Dysgraphia Dystonia Early-Onset Generalized Limb-Onset Dystonia Early-Onset Parkinson Disease Encephalitis Encephalopathy Eosinophilia-Myalgia Syndrome Ependymoma Epilepsy Epilepsy, Familial Adult Myoclonic, 2 Epilepsy, Familial Adult Myoclonic, 3 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure Erdheim-Chester Disease Essential Tremor Exophthalmos Fanconi Anemia, Complementation Group E Fmr1-Related Primary Ovarian Insufficiency Focal Dystonia Focal Epilepsy Fontaine Progeroid Syndrome Fragile X-Associated Tremor/ataxia Syndrome Fragile X Syndrome Fragile X Tremor/ataxia Syndrome Frontal Convexity Meningioma Frontotemporal Dementia Glaucoma-Related Pigment Dispersion Syndrome Glioma Hantavirus Pulmonary Syndrome Headache Hemifacial Spasm Hemiplegic Migraine Hepatic Adenomas, Familial Hereditary Ataxia Hereditary Late-Onset Parkinson Disease Huntington Disease Hydrocephalus Hyperkalemic Periodic Paralysis Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Olivary Degeneration Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoascorbemia Hypogonadism Hypokalemia Hypopituitarism Hypotonia Hypoxia Inclusion Body Myositis Infertility Inflammatory Bowel Disease Inner Ear Disease Internuclear Ophthalmoplegia Intracranial Hypotension Japanese Encephalitis Kwashiorkor L-2-Hydroxyglutaric Aciduria Laryngitis Lateral Sclerosis Learning Disability Leukodystrophy Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lingual-Facial-Buccal Dyskinesia Lipoid Proteinosis of Urbach and Wiethe Liver Cirrhosis Locked-in Syndrome Lymphoid Interstitial Pneumonia Machado-Joseph Disease Macroglobulinemia Malaria Megaloblastic Anemia Melanoma Microcephaly Mood Disorder Movement Disease Multiple Sclerosis Multiple System Atrophy 1 Muscle Hypertrophy Muscular Atrophy Myoclonus Myositis Neurodegeneration with Brain Iron Accumulation Neurodegeneration with Brain Iron Accumulation 1 Neurodegeneration with Brain Iron Accumulation 2a Neurodegeneration with Brain Iron Accumulation 3 Neuroleptic Malignant Syndrome Neuroma Neuronal Intranuclear Inclusion Disease Neuronitis Neuropathy Neurosarcoidosis Niemann-Pick Disease Niemann-Pick Disease, Type a Obsessive-Compulsive Disorder Obsessive-Compulsive Personality Disorder Obstructive Hydrocephalus Pancreatitis Paraneoplastic Cerebellar Degeneration Parkinson Disease 10 Parkinson Disease 15, Autosomal Recessive Early-Onset Parkinson Disease 2, Autosomal Recessive Juvenile Parkinson Disease 3, Autosomal Dominant Parkinson Disease, Late-Onset Pelizaeus-Merzbacher Disease Pellagra Personality Disorder Phenylketonuria Pick Disease of Brain Pilocytic Astrocytoma Pineal Cyst Plasmodium Vivax Malaria Pneumonia Polykaryocytosis Inducer Polyneuropathy Polyradiculoneuropathy Pontine Hemorrhage Postencephalitic Parkinson Disease Posttransplant Acute Limbic Encephalitis Primary Cerebellar Degeneration Primary Orthostatic Tremor Progressive Multifocal Leukoencephalopathy Prolidase Deficiency Prostatitis Proteus Syndrome Psychogenic Movement Ptosis Rem Sleep Behavior Disorder Restless Legs Syndrome Retinitis Rett Syndrome Roussy-Levy Hereditary Areflexic Dystasia Sarcoma Satb2-Associated Syndrome Scapuloperoneal Myopathy, X-Linked Dominant Scoliosis Sc Phocomelia Syndrome Segmental Dystonia Seizures, Benign Familial Neonatal, 1 Sleep Disorder Social Phobia Spasmodic Dysphonia Spastic Diplegia Spasticity Spastic Paraparesis Spinal Muscular Atrophy Spinocerebellar Ataxia 1 Spinocerebellar Ataxia, Autosomal Recessive 14 Spinocerebellar Degeneration Spontaneous Intracranial Hypotension Stiff-Person Syndrome Supranuclear Palsy, Progressive, 1 Sveinsson Chorioretinal Atrophy Synucleinopathy Tardive Dyskinesia Thoracic Outlet Syndrome Thrombocytosis Thyroiditis Tic Disorder Tooth Disease Torticollis Toxoplasmoză Traumatic Brain Injury Treacher Collins Syndrome 1 Tremor, Hereditary Essential, 2 Tremor, Hereditary Essential, and Idiopathic Normal Pressure Hydrocephalus Trisomy 1q Ulnar Neuropathy Ventricular Fibrillation, Paroxysmal Familial, 1 Vitamin B12 Deficiency Wernicke Encephalopathy West Nile Fever