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Nume Dementia
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Boli A-Z Aarskog-Scott Syndrome Achalasia Achromatopsia Acquired Immunodeficiency Syndrome Acquired Thrombocytopenia Acrocallosal Syndrome Acute Myocardial Infarction Acute Necrotizing Encephalopathy Type 1 Adenosine Deaminase 2 Deficiency Adrenoleukodystrophy Adult Polyglucosan Body Disease Age-Related Hearing Loss Aging Agnosia Agraphia Aids Dementia Complex Akinetic Mutism Aland Island Eye Disease Alcohol Abuse Alexia 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 Alzheimer Disease Alzheimer Disease 19 Alzheimer Disease 2 Alzheimer Disease 3 Alzheimer Disease 4 Amelogenesis Imperfecta Amusia Amyloidosis Amyloidosis, Hereditary, Transthyretin-Related Amyotrophic Lateral Sclerosis 1 Amyotrophic Lateral Sclerosis 18 Amyotrophic Lateral Sclerosis 21 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 Amyotrophic Lateral Sclerosis Type 14 Amyotrophic Lateral Sclerosis Type 6 Analbuminemia Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Aneurysm Aniridia 1 Anorexia Nervosa 1 Anosognosia Anterograde Amnesia Antiphospholipid Syndrome Antisocial Personality Disorder Aortic Valve Disease 2 Apert Syndrome Aphasia Apraxia Arachnoid Cysts Arachnoiditis Arteries, Anomalies of Arteriolosclerosis Arteriosclerosis Arteriovenous Fistula Arthrochalasia Ehlers-Danlos Syndrome Aspiration Pneumonia Associative Agnosia Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Atrial Fibrillation Atrophic Gastritis Autoimmune Encephalitis Autonomic Dysfunction Axonal Neuropathy Bacterial Meningitis Bacteriuria Basal Ganglia Calcification Basal Ganglia Disease B-Cell Lymphomas Behavioral Variant of Frontotemporal Dementia Bestrophinopathy, Autosomal Recessive Beta-Adrenergic Stimulation, Response to Binswanger's Disease Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borna Disease Brain Injury Brain Ischemia Branchiootic Syndrome 1 Brown-Vialetto-Van Laere Syndrome Bruxism Buerger Disease Bullous Pemphigoid C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Calcinosis Camurati-Engelmann Disease Capgras Syndrome Carcinoid Syndrome Carcinoid Tumors, Intestinal Cardiomyopathy, Familial Hypertrophic, 1 Carotid Artery Occlusion Carotid Stenosis Cataract Cat-Scratch Disease Central Nervous System Disease Central Nervous System Lymphoma Central Nervous System Tuberculosis Cerebellar Degeneration Cerebellar Disease Cerebral Amyloid Angiopathy, Cst3-Related Cerebral Amyloid Angiopathy, Itm2b-Related, 1 Cerebral Amyloid Angiopathy, Itm2b-Related, 2 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 Cerebral Arteriopathy, Autosomal Recessive, with Subcortical Infarcts and Leukoencephalopathy Cerebral Arteriosclerosis Cerebral Artery Occlusion Cerebral Atrophy Cerebral Degeneration Cerebral Hemorrhage Cerebral Hypoxia Cerebral Lipidosis Cerebral Lymphoma Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebroretinal Microangiopathy with Calcifications and Cysts 1 Cerebrotendinous Xanthomatosis Cerebrovascular Disease Cervical Dystonia Cervicitis Charles Bonnet Syndrome Chlamydia Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioretinitis Chronic Fatigue Syndrome Chronic Meningitis Citrullinemia, Classic Cocaine Abuse Cognitive Function 1, Social Cohen-Gibson Syndrome Colorblindness, Partial, Deutan Series Communicating Hydrocephalus Complex Regional Pain Syndrome Conduct Disorder Congestive Heart Failure Conversion Disorder Cortical Blindness Corticobasal Degeneration Creutzfeldt-Jakob Disease Critical Limb Ischemia Crouzon Syndrome with Acanthosis Nigricans Cystinuria Cytochrome P450 2d6 Variant Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Delusional Disorder Dementia, Lewy Body Dementia Pugilistica Dementia - Subcortical Demyelinating Polyneuropathy Dependent Personality Disorder Dermatitis Diabetes Mellitus Diarrhea Dnmt1-Related Dementia, Deafness, and Sensory Neuropathy Down Syndrome Dysautonomia Dysgraphia Dyslexia Dysphagia Dystonia Early-Onset, Autosomal Dominant Alzheimer Disease Early-Onset Familial Alzheimer Disease Early-Onset Parkinson Disease Echolalia Encephalitis Encephalomyopathy Encephalopathy Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endotheliitis Epididymo-Orchitis Epilepsy Essential Tremor Expressive Language Disorder Familial Acute Necrotizing Encephalopathy Familial Glucocorticoid Deficiency Familial Idiopathic Basal Ganglia Calcification Fanconi Anemia, Complementation Group E Fatal Familial Insomnia Fecal Incontinence Fetishism Fontaine Progeroid Syndrome Fragile X-Associated Tremor/ataxia Syndrome Frontotemporal Dementia Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia, Chromosome 3-Linked Frontotemporal Dementia with Parkinsonism-17 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related Gait Apraxia Galactose Epimerase Deficiency Gangliocytoma Gastritis Generalized Anxiety Disorder Genetic Prion Diseases Gerstmann-Straussler Disease Gingivitis Gitelman Syndrome Glaucoma-Related Pigment Dispersion Syndrome Gliomatosis Cerebri Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Griscelli Syndrome Grn-Related Frontotemporal Dementia Hansen's Disease Headache Head Injury Helicobacter Pylori Infection Hematologic Cancer Hemiplegia Hemolytic Anemia Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis C Hereditary Cerebral Amyloid Angiopathy Hereditary Sensory Neuropathy Hereditary Spastic Paraplegia Herpes Simplex Herpes Zoster Herpes Zoster Ophthalmicus Homocysteinemia Homocystinuria Human Herpesvirus 8 Human Immunodeficiency Virus Type 1 Huntington Disease Hydrocephalus Hyperacusis Hypercholesterolemia, Autosomal Dominant, 3 Hypereosinophilic Syndrome Hyperglycemia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hyperthyroidism Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypochondriasis Hypoglycemia Hypogonadotropism Hypomelanosis of Ito Hypoparathyroidism Hypopituitarism Hypothalamic Neoplasm Hypotonia Hypoxia Ideomotor Apraxia Immunodeficiency 43 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia Inclusion Body Myositis Insulin-Like Growth Factor I Internuclear Ophthalmoplegia Intestinal Tuberculosis Intracranial Aneurysm Intracranial Hypotension Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Intravascular Large B-Cell Lymphoma Ischemia Keratomalacia Kluver-Bucy Syndrome Kohlschutter-Tonz Syndrome Kufor-Rakeb Syndrome Lactic Acidosis Lateral Sclerosis Learning Disability Leber Hereditary Optic Neuropathy Lepromatous Leprosy Leukodystrophy Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukoencephalopathy with Vanishing White Matter Limb-Girdle Muscular Dystrophy Limbic Encephalitis Limb Ischemia Liver Cirrhosis Logopenic Progressive Aphasia Lymphoma Lymphopenia Machado-Joseph Disease Macrocytic Anemia Macs Syndrome Macular Dystrophy, Retinal, 1, North Carolina Type Major Affective Disorder 8 Major Affective Disorder 9 Malignant Spiradenoma Marchiafava Bignami Disease Mast Syndrome Meckel Syndrome, Type 1 Melancholia Meningioma, Familial Meningitis Meningoencephalitis Meningothelial Meningioma Meningovascular Neurosyphilis Metachromatic Leukodystrophy Mills Syndrome Mitochondrial Complex I Deficiency Mitochondrial Disorders Mitochondrial Encephalomyopathy Mitochondrial Import-Stimulating Factor Mood Disorder Motor Neuron Disease Movement Disease Mucolipidosis Iv Mucopolysaccharidosis Iii Mucopolysaccharidosis-Plus Syndrome Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple System Atrophy 1 Muscular Dystrophy Musical Perfect Pitch Mutism Myocardial Infarction Myoclonus Myoclonus and Ataxia Myoclonus Epilepsy Myopathy Myotonic Dystrophy 2 Myxedema Narcissistic Personality Disorder Nervous System Disease Neuritis Neuroaxonal Dystrophy Neurodegeneration with Brain Iron Accumulation Neurodegeneration with Brain Iron Accumulation 2a Neuroleptic Malignant Syndrome Neuromuscular Disease Neuronal Ceroid-Lipofuscinoses Neuronal Ceroid Lipofuscinosis Neuronitis Neuropathy Neuropathy, Hereditary Sensory, Type Ie Neurosarcoidosis Neurosyphilis Niemann-Pick Disease Nominal Aphasia Obesity, Hyperphagia, and Developmental Delay Obsessive-Compulsive Disorder Obstructive Hydrocephalus Ocular Motor Apraxia Oculopharyngeal Muscular Dystrophy Olivopontocerebellar Atrophy Omenn Syndrome Open-Angle Glaucoma Opitz Gbbb Syndrome, Type I Orchitis Orthostatic Intolerance Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Ovalocytosis, Southeast Asian Paine Syndrome Pandas Parametritis Paranoid Schizophrenia Paraplegia Parkinson-Dementia Syndrome Parkinson Disease 10 Parkinson Disease 15, Autosomal Recessive Early-Onset Parkinson Disease 2, Autosomal Recessive Juvenile Parkinson Disease 3, Autosomal Dominant Parkinson Disease 7, Autosomal Recessive Early-Onset Parkinson Disease, Late-Onset Parkinson Disease Type 9 Pathological Gambling Pedophilia Pellagra Peptic Ulcer Disease Periodontitis Perioral Myoclonia with Absences Peritonitis Pernicious Anemia Perry Syndrome Persistent Vegetative State Personality Disorder Phenylketonuria Phonagnosia Pica Disease Pick Disease of Brain Pituitary Hormone Deficiency, Combined, 2 Platelet Membrane Fluidity Pneumonia Pneumothorax, Primary Spontaneous Polycystic Kidney Disease Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy Polykaryocytosis Inducer Polyneuropathy Postencephalitic Parkinson Disease Posterior Cortical Atrophy Postpartum Depression Post-Traumatic Stress Disorder Prader-Willi Syndrome Premature Ovarian Failure 7 Primary Angiitis of the Central Nervous System Primary Central Nervous System Lymphoma Primary Optic Atrophy Prion Disease Progressive Myoclonus Epilepsy Progressive Non-Fluent Aphasia Propionic Acidemia Prosopagnosia Pseudobulbar Affect Pseudobulbar Palsy Pseudohypoparathyroidism Pulmonary Fibrosis, Idiopathic Pulmonary Sarcoidosis Pure Autonomic Failure Purpura Raine Syndrome Relapsing Polychondritis Rem Sleep Behavior Disorder Renal Glucosuria Renal Nutcracker Syndrome Renovascular Hypertension Retinal Degeneration Retinal Disease Retinitis Retinitis Pigmentosa Retrograde Amnesia Rosacea Salt and Pepper Developmental Regression Syndrome Sarcoid Meningitis Sarcoidosis 2 Sarcoma Scabies Scapuloperoneal Myopathy, X-Linked Dominant Schizoaffective Disorder Schizophrenia Schizophreniform Disorder Scoliosis, Isolated 1 Semantic Dementia Senile Plaque Formation Sensory Neuropathy Type 1 Siderosis Simultanagnosia Sjogren-Larsson Syndrome Sleep Apnea Sleep Disorder Sneddon Syndrome Solitary Bone Cyst Somatization Disorder Spasticity Spastic Paraparesis Spastic Pseudosclerosis Speech and Communication Disorders Spinal Meningioma Spontaneous Intracranial Hypotension Striatonigral Degeneration Subacute Delirium Subclavian Steal Syndrome Subcortical Arteriosclerotic Encephalopathy Substance Abuse Sudden Arrhythmia Death Syndrome Superficial Siderosis Superficial Siderosis of the Central Nervous System Suprabulbar Paresis, Congenital Supranuclear Palsy, Progressive, 1 Sveinsson Chorioretinal Atrophy Syncope Synucleinopathy Syphilis Tardive Dyskinesia Temporal Arteritis Temporal Lobe Epilepsy Thrombocytopenia Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Toxic Encephalopathy Toxoplasmoză Transient Global Amnesia Traumatic Brain Injury Treacher Collins Syndrome 1 Tremor Trichotillomania Tuberous Sclerosis Vascular Dementia Vascular Disease Velocardiofacial Syndrome Vertebrobasilar Insufficiency Visual Agnosia Vitamin B12 Deficiency Wernicke-Korsakoff Syndrome Whipple Disease Xanthomatosis