Informaţii despre

Nume Pick Disease of Brain
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Dementia in Pick disease
Clasificare anatomică Malacards Boli neuronale; Boli psihice

Vezi şi

Boli A-Z Adie Pupil Aging Agraphia Alexia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Alzheimer Disease Alzheimer Disease 2 Alzheimer Disease 3 Alzheimer Disease 4 Amyloidosis Amyotrophic Lateral Sclerosis 1 Amyotrophic Lateral Sclerosis 11 Amyotrophic Lateral Sclerosis 18 Amyotrophic Lateral Sclerosis 21 Amyotrophic Lateral Sclerosis Type 14 Amyotrophic Lateral Sclerosis Type 6 Anauxetic Dysplasia 1 Aniridia 1 Anorexia Nervosa 1 Aortic Valve Disease 2 Aphasia Apraxia Argyria Arthrochalasia Ehlers-Danlos Syndrome Associative Agnosia Astrocytoma Basal Ganglia Disease Behavioral Variant of Frontotemporal Dementia Binswanger's Disease Blood Group--Ahonen Cerebellar Astrocytoma Cerebral Amyloid Angiopathy, Cst3-Related Cerebritis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Colorblindness, Partial, Deutan Series Conjunctivitis Constrictive Pericarditis Corticobasal Degeneration Cranial Nerve Malignant Neoplasm Creutzfeldt-Jakob Disease Dementia Dementia, Lewy Body Down Syndrome Early-Onset, Autosomal Dominant Alzheimer Disease Early-Onset Familial Alzheimer Disease Echolalia Expressive Language Disorder Familial Idiopathic Basal Ganglia Calcification Frontotemporal Dementia Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related Gait Apraxia Glaucoma-Related Pigment Dispersion Syndrome Head Injury Hemorrhage, Intracerebral Hepatic Adenomas, Familial Hydrocephalus Hydrocephalus, Normal-Pressure Ideomotor Apraxia Inclusion Body Myositis Kluver-Bucy Syndrome Lateral Sclerosis Lethal Congenital Contracture Syndrome 1 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lipoprotein Glomerulopathy Liver Disease Loeys-Dietz Syndrome 3 Motor Neuron Disease Multiple System Atrophy 1 Myoclonus Myopathy, Myofibrillar, 1 Myopathy, Myofibrillar, 2 Nervous System Disease Neuronal Intranuclear Inclusion Disease Neuronitis Nominal Aphasia Obsessive-Compulsive Disorder Olfactory Nerve Neoplasm Olivopontocerebellar Atrophy Parkinson Disease 3, Autosomal Dominant Pelvic Inflammatory Disease Pericarditis Perry Syndrome Phonagnosia Postencephalitic Parkinson Disease Posterior Cortical Atrophy Primary Progressive Apraxia of Speech Prion Disease Progressive Non-Fluent Aphasia Prolidase Deficiency Prosopagnosia Rem Sleep Behavior Disorder Schizophrenia Semantic Dementia Senile Plaque Formation Speech and Communication Disorders Spondyloocular Syndrome Supranuclear Palsy, Progressive, 1 Synucleinopathy Tay-Sachs Disease Tremor Trichohepatoenteric Syndrome 1 Undifferentiated Pleomorphic Sarcoma Vascular Dementia Writing Disorder