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Genopedia


C9orf72
71 disease terms (MeSH) has been reported with C9orf72 gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Amyotrophic Lateral Sclerosis Phenopedia 128 4
    Frontotemporal Dementia Phenopedia 82 2
    Frontotemporal Lobar Degeneration Phenopedia 30 2
    Alzheimer Disease Phenopedia 21 0
    Neuropsychological Tests Phenopedia 18 0
    Disease Progression Phenopedia 13 0
    Cognition Disorders Phenopedia 12 0
    Atrophy Phenopedia 12 0
    Motor Neuron Disease Phenopedia 12 1
    Parkinson Disease Phenopedia 9 0
    Dementia Phenopedia 9 0
    Psychotic Disorders Phenopedia 7 0
    Schizophrenia Phenopedia 5 0
    TDP-43 Proteinopathies Phenopedia 5 0
    Aphasia, Primary Progressive Phenopedia 5 0
    Neurodegenerative Diseases Phenopedia 5 1
    Spinocerebellar Ataxias Phenopedia 3 0
    Huntington Disease Phenopedia 3 0
    Multiple Sclerosis Phenopedia 3 0
    Supranuclear Palsy, Progressive Phenopedia 3 0
    Basal Ganglia Diseases Phenopedia 3 0
    Genomic Instability Phenopedia 2 0
    Cognition Phenopedia 2 0
    Primary Progressive Nonfluent Aphasia Phenopedia 2 0
    Muscular Atrophy, Spinal Phenopedia 2 0
    Paraplegia Phenopedia 2 0
    Schizophrenic Psychology Phenopedia 2 0
    Mental Status Schedule Phenopedia 2 0
    Cerebellar Diseases Phenopedia 1 0
    Psychomotor Performance Phenopedia 1 0
    Wechsler Scales Phenopedia 1 0
    Apraxias Phenopedia 1 0
    Hydrocephalus, Normal Pressure Phenopedia 1 0
    Muscular Dystrophy, Emery-Dreifuss Phenopedia 1 0
    Nerve Degeneration Phenopedia 1 0
    Pick Disease of the Brain Phenopedia 1 0
    Psychometrics Phenopedia 1 0
    Neoplasms Phenopedia 1 0
    Ataxia Phenopedia 1 1
    Aphasia Phenopedia 1 0
    Arthritis, Rheumatoid Phenopedia 1 0
    Attention Phenopedia 1 0
    Cerebral Hemorrhage Phenopedia 1 0
    Inflammation Phenopedia 1 0
    Memory, Short-Term Phenopedia 1 0
    Multiple System Atrophy Phenopedia 1 0
    Spastic Paraplegia, Hereditary Phenopedia 1 0
    Mental Disorders Phenopedia 1 0
    Depressive Disorder Phenopedia 1 0
    Inhibition (Psychology) Phenopedia 1 0
    Mental Recall Phenopedia 1 0
    Autistic Disorder Phenopedia 1 0
    Executive Function Phenopedia 1 0
    Perceptual Disorders Phenopedia 1 0
    Sclerosis Phenopedia 1 0
    Spinocerebellar Degenerations Phenopedia 1 0
    Alcoholism Phenopedia 1 0
    Multiple Sclerosis, Chronic Progressive Phenopedia 1 0
    Asymptomatic Diseases Phenopedia 1 0
    Bone Cysts Phenopedia 1 0
    Heredodegenerative Disorders, Nervous System Phenopedia 1 0
    Machado-Joseph Disease Phenopedia 1 0
    Myositis, Inclusion Body Phenopedia 1 0
    Psychiatric Status Rating Scales Phenopedia 1 0
    Syndrome Phenopedia 1 1
    REM Sleep Behavior Disorder Phenopedia 1 0
    Parkinsonian Disorders Phenopedia 1 0
    Auditory Perception Phenopedia 1 0
    Myopathies, Structural, Congenital Phenopedia 1 0
    Nervous System Diseases Phenopedia 1 0
    Amnesia 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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