Informaţii despre

Nume Frontotemporal Dementia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Circumscribed brain atrophy
Clasificare anatomică Malacards Boli neuronale; Boli psihice

Vezi şi

Boli A-Z Acute Disseminated Encephalomyelitis Adie Pupil Aging Agnosia Agraphia 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 2 Alzheimer Disease 3 Alzheimer Disease 4 Amusia Amyotrophic Lateral Sclerosis 1 Amyotrophic Lateral Sclerosis 18 Amyotrophic Lateral Sclerosis 21 Amyotrophic Lateral Sclerosis Type 14 Amyotrophic Lateral Sclerosis Type 6 Anauxetic Dysplasia 1 Aneurysm Aniridia 1 Anorexia Nervosa 1 Anosognosia Anterograde Amnesia Aphasia Apraxia Arthrochalasia Ehlers-Danlos Syndrome Associative Agnosia Autonomic Dysfunction Basal Ganglia Disease Behavioral Variant of Frontotemporal Dementia Beta-Adrenergic Stimulation, Response to Binswanger's Disease Bipolar Disorder Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brain Injury Brown-Vialetto-Van Laere Syndrome C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Calcinosis Cardiomyopathy, Familial Hypertrophic, 1 Cerebral Amyloid Angiopathy, Cst3-Related Cerebral Atrophy Cerebral Hemorrhage Cerebritis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Citrullinemia, Classic Cognitive Function 1, Social Conjunctivitis Corticobasal Degeneration Creutzfeldt-Jakob Disease Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Dementia Dementia, Lewy Body Dementia - Subcortical Dyslexia Dystonia Early-Onset, Autosomal Dominant Alzheimer Disease Early-Onset Familial Alzheimer Disease Echolalia Expressive Language Disorder Familial Idiopathic Basal Ganglia Calcification Fanconi Anemia, Complementation Group E Fontaine Progeroid Syndrome 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 Gangliocytoma Genetic Prion Diseases Grn-Related Frontotemporal Dementia Hepatic Adenomas, Familial Hydrocephalus Ideomotor Apraxia Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia Inclusion Body Myositis Intracranial Hypotension Kluver-Bucy Syndrome Lateral Sclerosis Leukoencephalopathy, Hereditary Diffuse, with Spheroids Limb-Girdle Muscular Dystrophy Machado-Joseph Disease Major Affective Disorder 8 Major Affective Disorder 9 Motor Neuron Disease Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple System Atrophy 1 Muscular Dystrophy Musical Perfect Pitch Mutism Myoclonus Myopathy Myotonic Dystrophy 2 Narcissistic Personality Disorder Neuromuscular Disease Neuronal Ceroid Lipofuscinosis Neuronal Intranuclear Inclusion Disease Neuronitis Nominal Aphasia Obsessive-Compulsive Disorder Parkinson Disease 3, Autosomal Dominant Pathological Gambling Pedophilia Perry Syndrome Personality Disorder Phonagnosia Pick Disease of Brain Polykaryocytosis Inducer Postencephalitic Parkinson Disease Posterior Cortical Atrophy Postpartum Depression Prion Disease Progressive Non-Fluent Aphasia Rem Sleep Behavior Disorder Salt and Pepper Developmental Regression Syndrome Sarcoma Scapuloperoneal Myopathy, X-Linked Dominant Schizophrenia Semantic Dementia Senile Plaque Formation Speech and Communication Disorders Spinocerebellar Ataxia 31 Spontaneous Intracranial Hypotension Substance Abuse Supranuclear Palsy, Progressive, 1 Synucleinopathy Traumatic Brain Injury Tremor Trichohepatoenteric Syndrome 1 Tuberous Sclerosis Vascular Dementia Vascular Disease Visual Agnosia Vitamin B12 Deficiency