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Genopedia


MAPT

92 disease terms (MeSH) has been reported with MAPT gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Parkinson Disease Phenopedia 92 9
    Alzheimer Disease Phenopedia 67 11
    Dementia Phenopedia 40 5
    Frontotemporal Dementia Phenopedia 27 0
    Supranuclear Palsy, Progressive Phenopedia 22 0
    Disease Progression Phenopedia 17 3
    Neuropsychological Tests Phenopedia 17 1
    Cognition Disorders Phenopedia 13 1
    Neurodegenerative Diseases Phenopedia 12 1
    Atrophy Phenopedia 11 1
    Tauopathies Phenopedia 10 1
    Cognition Phenopedia 8 1
    Frontotemporal Lobar Degeneration Phenopedia 6 0
    Lewy Body Disease Phenopedia 6 1
    Parkinsonian Disorders Phenopedia 5 1
    Amyotrophic Lateral Sclerosis Phenopedia 5 0
    Aphasia, Primary Progressive Phenopedia 4 0
    Mental Status Schedule Phenopedia 4 1
    Schizophrenia Phenopedia 4 0
    Psychotic Disorders Phenopedia 3 0
    Syndrome Phenopedia 3 2
    Multiple System Atrophy Phenopedia 3 0
    Neoplasms Phenopedia 3 0
    Nerve Degeneration Phenopedia 3 0
    Memory Phenopedia 3 0
    Plaque, Amyloid Phenopedia 3 0
    Primary Progressive Nonfluent Aphasia Phenopedia 3 0
    Dementia, Vascular Phenopedia 3 1
    Creutzfeldt-Jakob Syndrome Phenopedia 3 0
    Essential Tremor Phenopedia 2 0
    Depressive Disorder, Major Phenopedia 2 0
    Bipolar Disorder Phenopedia 2 0
    Psychomotor Performance Phenopedia 2 0
    Psychiatric Status Rating Scales Phenopedia 2 1
    Hallucinations Phenopedia 2 0
    Huntington Disease Phenopedia 2 0
    Imagination Phenopedia 1 0
    Inhibition (Psychology) Phenopedia 1 0
    Inversion, Chromosome Phenopedia 1 0
    Memory Disorders Phenopedia 1 0
    Mental Retardation Phenopedia 1 0
    Myocardial Infarction Phenopedia 1 0
    Metabolic Syndrome X Phenopedia 1 0
    Motor Neuron Disease Phenopedia 1 0
    Mouth Abnormalities Phenopedia 1 0
    Movement Disorders Phenopedia 1 0
    Multiple Sclerosis Phenopedia 1 0
    Psychometrics Phenopedia 1 0
    Psychomotor Disorders Phenopedia 1 1
    Prion Diseases Phenopedia 1 0
    Prostatic Neoplasms Phenopedia 1 0
    Perceptual Disorders Phenopedia 1 0
    Peripheral Nervous System Diseases Phenopedia 1 0
    Pick Disease of the Brain Phenopedia 1 0
    Niemann-Pick Disease, Type C Phenopedia 1 0
    Optic Atrophy, Hereditary, Leber Phenopedia 1 0
    Osteoporosis Phenopedia 1 0
    Ovarian Neoplasms Phenopedia 1 0
    Blindness Phenopedia 1 0
    Brain Concussion Phenopedia 1 0
    Brain Diseases Phenopedia 1 0
    Brain Injury, Chronic Phenopedia 1 0
    Brain Ischemia Phenopedia 1 0
    Cardiovascular Diseases Phenopedia 1 0
    Carotid Stenosis Phenopedia 1 0
    Cerebellar Ataxia Phenopedia 1 0
    Child Development Disorders, Pervasive Phenopedia 1 0
    Chromosome Inversion Phenopedia 1 1
    Cleft Lip Phenopedia 1 0
    Cleft Palate Phenopedia 1 0
    Anxiety Disorders Phenopedia 1 0
    Aphasia Phenopedia 1 0
    Amnesia Phenopedia 1 0
    Amyloidosis Phenopedia 1 0
    Auditory Perception Phenopedia 1 0
    Autistic Disorder Phenopedia 1 0
    Basal Ganglia Diseases Phenopedia 1 0
    Diabetes Complications Phenopedia 1 0
    Asymptomatic Diseases Phenopedia 1 0
    Atherosclerosis Phenopedia 1 0
    Craniocerebral Trauma Phenopedia 1 0
    Craniofacial Abnormalities Phenopedia 1 0
    Crohn Disease Phenopedia 1 0
    Dystonia Phenopedia 1 1
    REM Sleep Behavior Disorder Phenopedia 1 0
    Restless Legs Syndrome Phenopedia 1 0
    Space Perception Phenopedia 1 0
    Thrombosis Phenopedia 1 0
    Tourette Syndrome Phenopedia 1 0
    Tremor Phenopedia 1 0
    Vision Disorders Phenopedia 1 0
    Visual Perception Phenopedia 1 0
Note: The number of publications displayed in this table will differ from the number displayed in the HuGE Literature Finder as the number in Genopedia reflects only the indexed disease term without children terms, but the number in the HuGE Literature Finder reflects all text searches of the disease term including the indexed term and corresponding children terms.
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