Informaţii despre

Nume Alzheimer Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Alzheimer disease with early onset; Alzheimer disease with late onset; Alzheimer disease, unspecified; Dementia in Alzheimer disease with early onset; Dementia in Alzheimer disease with late onset; Dementia in Alzheimer disease, unspecified
Clasificare anatomică Malacards Boli neuronale; Boli psihice
Boli din aceeaşi familie Alzheimer Disease 10; Alzheimer Disease 11; Alzheimer Disease 12; Alzheimer Disease 13; Alzheimer Disease 14; Alzheimer Disease 15; Alzheimer Disease 16; Alzheimer Disease 17; Alzheimer Disease 18; Alzheimer Disease 19; Alzheimer Disease 2; Alzheimer Disease 3; Alzheimer Disease 4; Alzheimer Disease 5; Alzheimer Disease 6; Alzheimer Disease 7; Alzheimer Disease 8; Alzheimer Disease 9; Alzheimer Disease Type 1; Early-Onset Familial Alzheimer Disease; Early-Onset, Autosomal Dominant Alzheimer Disease

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Boli A-Z Aarskog-Scott Syndrome Achromatopsia Acquired Thrombocytopenia Acrocallosal Syndrome Acute Disseminated Encephalomyelitis Acute Vascular Insufficiency of Intestine Adenoma Adie Pupil Adiponectin, Serum Level of, Quantitative Trait Locus 1 Aging Agnosia Agraphia Aids Dementia Complex Akinetopsia Aland Island Eye Disease Alcohol Abuse Alcohol Dependence Alexander Disease Alexia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Universalis Congenita Alpha-2-Macroglobulin Deficiency 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 10 Alzheimer Disease 11 Alzheimer Disease 12 Alzheimer Disease 13 Alzheimer Disease 14 Alzheimer Disease 15 Alzheimer Disease 16 Alzheimer Disease 17 Alzheimer Disease 19 Alzheimer Disease 2 Alzheimer Disease 3 Alzheimer Disease 4 Alzheimer Disease 5 Alzheimer Disease 6 Alzheimer Disease 7 Alzheimer Disease 8 Alzheimer Disease Mitochondrial Alzheimer Disease Type 1 Amusia Amyloidosis Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome Androgen Insensitivity Syndrome, Mild Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Anosognosia Aortic Atherosclerosis Aortic Valve Disease 2 Apert Syndrome Aphasia Apocrine Gland Secretion, Variation in Apolipoprotein C-Iii Deficiency Apraxia Argyria Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aspiration Pneumonia Associative Agnosia Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Athetosis Audiogenic Seizures Aural Atresia, Congenital Autoimmune Disease Autoimmune Inner Ear Disease Autonomic Dysfunction Axenfeld-Rieger Syndrome Behavioral Variant of Frontotemporal Dementia 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 Blood Group--Swann System Bloom 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bornholm Eye Disease Brain Cancer Brain Injury Brain Ischemia Brain Meningioma Breast Adenocarcinoma Breast Cancer Bullous Pemphigoid Buruli Ulcer Capgras Syndrome Cataract Cd45 Deficiency Central Nervous System Disease Cerebellar Astrocytoma Cerebellar Degeneration Cerebral Amyloid Angiopathy, Cst3-Related Cerebral Amyloid Angiopathy, Itm2b-Related, 1 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 Cerebral Arteriosclerosis Cerebral Artery Occlusion Cerebral Atherosclerosis Cerebral Atrophy Cerebral Degeneration Cerebral Hemorrhage Cerebritis Cerebroretinal Microangiopathy with Calcifications and Cysts 1 Cerebrovascular Disease Ceroid Lipofuscinosis, Neuronal, 10 Ceroid Lipofuscinosis, Neuronal, 5 Cervical Dystonia Cervicitis Chiari Malformation Childhood Myocerebrohepatopathy Spectrum Chlamydia Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Choroiditis Chromosomal Triplication Chromosome 16 Trisomy Ciliary Dyskinesia, Primary, 1 Citrullinemia, Classic Cognitive Function 1, Social Collecting Duct Carcinoma Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congestive Heart Failure Conjunctivitis Corticobasal Degeneration Creutzfeldt-Jakob Disease Crouzon Syndrome with Acanthosis Nigricans Cystic Fibrosis Cytochrome P450 2d6 Variant Cytomegalovirus Infection Dementia Dementia, Lewy Body Dementia Pugilistica Dementia - Subcortical Diabetes Mellitus Diabetic Encephalopathy Differentiating Neuroblastoma Dihydropyrimidinase Deficiency Disease_ontology Down Syndrome Drug Dependence Dysautonomia Dyscalculia Dysembryoplastic Neuroepithelial Tumor Dysgraphia Dysphagia Dystonia Dystrophinopathies Early-Onset, Autosomal Dominant Alzheimer Disease Early-Onset Familial Alzheimer Disease Early-Onset Schizophrenia Eating Disorder Eclampsia Ectopic Pregnancy Embryonal Carcinoma Encephalitis Encephalomalacia Encephalopathy Endotheliitis Eosinophilic Gastroenteritis Epilepsy Epithelial Recurrent Erosion Dystrophy Essential Tremor Exfoliation Syndrome Exocrine Pancreatic Insufficiency Factor Xii Deficiency Familial Adenomatous Polyposis 1 Familial Idiopathic Basal Ganglia Calcification Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Fatal Familial Insomnia Fetal Akinesia Deformation Sequence Finger Agnosia Focal Segmental Glomerulosclerosis Fragile X-Associated Tremor/ataxia Syndrome Fragile X Syndrome Friedreich Ataxia 1 Frontotemporal Dementia Fundus Albipunctatus Gaba Aminotransferase Deficiency Gait Apraxia Ganglioglioma Genitopatellar Syndrome Gerstmann Syndrome Gestational Diabetes Gitelman Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioblastoma Multiforme Glucose Intolerance Glucose Metabolism Disease Glucose Transporter Type 1 Deficiency Syndrome Gout Granular Cell Tumor Griscelli Syndrome Headache Headache Associated with Sexual Activity Head Injury Hematologic Cancer Hemiparkinsonism-Hemiatrophy Syndrome Hemorrhage, Intracerebral Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatocellular Carcinoma Hereditary Wilms' Tumor Herpes Simplex Herpes Simplex Encephalitis Hidradenitis Hidradenitis Suppurativa Hinman Syndrome Histiocytosis-Lymphadenopathy Plus Syndrome Histrionic Personality Disorder Homocysteinemia Horns in Sheep Huntington Disease Hydrocephalus Hypercholesterolemia, Autosomal Dominant, 3 Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoganglionosis Hypophosphatasia, Adult Hypophosphatasia, Infantile Hypoxia Ideomotor Apraxia Immunodeficiency with Hyper-Igm, Type 3 Immunoglobulin E Concentration, Serum Inclusion Body Myositis Insulin-Like Growth Factor I Intellectual Disability-Developmental Delay-Contractures Syndrome Irritable Bowel Syndrome Ischemia Isolated Optic Neuritis Jejunoileitis Kuru Lateral Sclerosis Learning Disability Leukemia Leukodystrophy Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leydig Cell Hypoplasia, Type I Limbic Encephalitis Lissencephaly 1 Liver Disease Logopenic Progressive Aphasia Long Qt Syndrome 15 Lymphoblastic Leukemia Macs Syndrome Malaria Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Meningitis Meningoencephalitis Metachromatic Leukodystrophy Microcephaly Migraine with or Without Aura 1 Mirage Syndrome Mohr-Tranebjaerg Syndrome Mood Disorder Motor Neuron Disease Muir-Torre Syndrome Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple System Atrophy 1 Mungan Syndrome Muscular Dystrophy Musical Perfect Pitch Myd88 Deficiency Myeloid Leukemia Myiasis Myocardial Infarction Myoclonus Myoclonus Epilepsy Myositis Narcolepsy Nervous System Disease Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neuroaxonal Dystrophy Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Neuropathy Neurosyphilis Neutrophil Actin Dysfunction Niemann-Pick Disease Obsessive-Compulsive Disorder Ocular Dominance Olivopontocerebellar Atrophy Open-Angle Glaucoma Opitz Gbbb Syndrome, Type Ii Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis Pachyonychia Congenita 2 Palmomental Reflex Pancreatitis Parametritis Parkinson Disease 15, Autosomal Recessive Early-Onset Parkinson Disease 2, Autosomal Recessive Juvenile Parkinsonism with Spasticity, X-Linked Persistent Vegetative State Personality Disorder Pertussis Pfeiffer Syndrome Phenylketonuria Phonagnosia Pick Disease of Brain Platelet Membrane Fluidity Pneumoconiosis Pneumonia Polymorphic Reticulosis Porphyria Postencephalitic Parkinson Disease Posterior Cortical Atrophy Postural Hypotension Prader-Willi Syndrome Pre-Eclampsia Premature Centromere Division Premature Chromatid Separation Trait Prieto X-Linked Mental Retardation Syndrome Primary Angiitis of the Central Nervous System Prion Disease Progressive Myoclonus Epilepsy Progressive Non-Fluent Aphasia Prosopagnosia Prostate Cancer Prostatitis Proteus Syndrome Prurigo Nodularis Pseudobulbar Affect Pseudocholinesterase Deficiency Pure Autonomic Failure Raine Syndrome Ramer Ladda Syndrome Rem Sleep Behavior Disorder Renal Glucosuria Renal Nutcracker Syndrome Renovascular Hypertension Restless Legs Syndrome Retinal Degeneration Retinal Dysplasia, Primary Retinitis Retinoschisis 1, X-Linked, Juvenile Retrograde Amnesia Reye Syndrome Rheumatoid Arthritis Root Caries Salivary Gland Adenoma, Pleomorphic Salt and Pepper Developmental Regression Syndrome Schizophrenia Scoliosis, Isolated 1 Sc Phocomelia Syndrome Scrapie Secondary Progressive Multiple Sclerosis Semantic Dementia Senile Plaque Formation Short Stature, Developmental Delay, and Congenital Heart Defects Sick Sinus Syndrome Siderosis Sleep Apnea Spasticity Spastic Paraparesis Spastic Paraplegia, Ataxia, and Mental Retardation Spinal Cord Injury Spinocerebellar Ataxia 2 Status Epilepticus Striatonigral Degeneration Stuve-Wiedemann Syndrome Substance Dependence Superficial Siderosis Supranuclear Palsy, Progressive, 1 Sveinsson Chorioretinal Atrophy Sweat Gland Disease Synucleinopathy Syringomyelia Tardive Dyskinesia Tay-Sachs Disease Temporal Lobe Epilepsy Teratocarcinoma Tetanus Tetraploidy Thrombosis Thyroid Cancer, Nonmedullary, 1 Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Toxic Encephalopathy Transient Cerebral Ischemia Transsexualism Transsexuality Traumatic Brain Injury Tremor Trichohepatoenteric Syndrome 1 Trigeminal Trophic Syndrome Tropical Calcific Pancreatitis Ulna and Fibula, Absence of, with Severe Limb Deficiency Undifferentiated Pleomorphic Sarcoma Vaccinia Vascular Dementia Vascular Disease Vertebrobasilar Insufficiency Visual Agnosia Vitamin B12 Deficiency Wegener Granulomatosis Wernicke Encephalopathy Wernicke-Korsakoff Syndrome Williams-Beuren Syndrome Wilms Tumor 6 Wilson Disease Wiskott-Aldrich Syndrome Wolf-Hirschhorn Syndrome Writing Disorder