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Nume Aphasia
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Boli A-Z Ablepharon-Macrostomia Syndrome Acute Disseminated Encephalomyelitis Aging Agnosia Agraphia Akinetic Mutism Aland Island Eye Disease Alexia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease Alzheimer Disease 2 Alzheimer Disease 4 Amusia Aniridia 1 Anorexia Nervosa 1 Anosognosia Anterior Cerebral Artery Infarction Apraxia Arteriovenous Fistula Arthrochalasia Ehlers-Danlos Syndrome Aseptic Meningitis Associative Agnosia Astrocytoma Atrial Fibrillation Auditory Agnosia Autotopagnosia Basal Ganglia Disease Behavioral Variant of Frontotemporal Dementia Binswanger's Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Cerebellar Disease Cerebral Amyloid Angiopathy, Cst3-Related Cerebral Atrophy Cerebral Hemorrhage Cerebritis Cervicitis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choroiditis Chronic Myelomonocytic Leukemia Cognitive Function 1, Social Cognitive Impairment with or Without Cerebellar Ataxia Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Cortical Blindness Corticobasal Degeneration Cranial Nerve Palsy Creutzfeldt-Jakob Disease Crouzon Syndrome with Acanthosis Nigricans Dementia Dementia, Lewy Body Dysgraphia Dyslexia Dyslexia 1 Dysphagia Early-Onset, Autosomal Dominant Alzheimer Disease Early-Onset Familial Alzheimer Disease Early-Onset Parkinson Disease Echolalia Encephalitis Encephalopathy Endogenous Depression Epilepsy Epilepsy-Aphasia Spectrum Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation Expressive Language Disorder Familial Idiopathic Basal Ganglia Calcification Fanconi Anemia, Complementation Group E Focal Epilepsy Foix Chavany Marie Syndrome Frontotemporal Dementia Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related Gait Apraxia Genetic Prion Diseases Gerstmann-Straussler Disease Gerstmann Syndrome Glioma Hantavirus Pulmonary Syndrome Headache Head Injury Hemiplegia Hemorrhage, Intracerebral Hepatic Encephalopathy Hepatitis Hereditary Late-Onset Parkinson Disease Herpes Simplex Herpes Simplex Encephalitis Hydrocephalus, Normal-Pressure Hyperostosis Hypotonia Ideomotor Apraxia Inclusion Body Myositis Kawasaki Disease Kernicterus Kluver-Bucy Syndrome Landau-Kleffner Syndrome Lateral Sclerosis Learning Disability Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Logopenic Progressive Aphasia Lymphoblastic Leukemia Macroglobulinemia Malaria Marchiafava Bignami Disease Meningitis Middle Cerebral Artery Infarction Miliary Tuberculosis Mills Syndrome Mononeuritis Multiplex Motor Neuron Disease Movement Disease Multiple System Atrophy 1 Mutism Nephrotic Syndrome Nervous System Disease Neurodegeneration with Brain Iron Accumulation 2a Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronitis Nominal Aphasia Non-Syndromic X-Linked Intellectual Disability Otitis Media Ovarian Hyperstimulation Syndrome Parkinson Disease 10 Parkinson Disease 2, Autosomal Recessive Juvenile Parkinson Disease 3, Autosomal Dominant Parkinsonism-Dystonia, Infantile Pdgfrb-Associated Chronic Eosinophilic Leukemia Perry Syndrome Pervasive Developmental Disorder Phonagnosia Pick Disease of Brain Postencephalitic Parkinson Disease Posterior Cortical Atrophy Premature Chromatid Separation Trait Primary Progressive Apraxia of Speech Prion Disease Progressive Non-Fluent Aphasia Prosopagnosia Protein S Deficiency Quadriplegia Rapp-Hodgkin Syndrome Reading Disorder Rem Sleep Behavior Disorder Salt and Pepper Developmental Regression Syndrome Seizure Disorder Semantic Dementia Senile Plaque Formation Speech and Communication Disorders Speech Disorder Status Epilepticus Suppurative Otitis Media Supranuclear Palsy, Progressive, 1 Sveinsson Chorioretinal Atrophy Swallowing Disorders Synucleinopathy Tactile Agnosia Thrombosis Toxic Encephalopathy Transient Global Amnesia Tremor Typhoid Fever Vascular Dementia Visual Agnosia Vohwinkel Syndrome, Variant Form Writing Disorder