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Genopedia


FMR1

74 disease terms (MeSH) has been reported with FMR1 gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Fragile X Syndrome Phenopedia 77 0
    Primary Ovarian Insufficiency Phenopedia 26 1
    Tremor Phenopedia 19 0
    Ovarian Failure, Premature Phenopedia 16 0
    Ataxia Phenopedia 16 0
    Infertility, Female Phenopedia 12 0
    Neuropsychological Tests Phenopedia 11 0
    Autistic Disorder Phenopedia 7 0
    Parkinson Disease Phenopedia 7 0
    Parkinsonian Disorders Phenopedia 6 0
    Schizophrenia Phenopedia 5 0
    Menopause, Premature Phenopedia 5 0
    Cognition Phenopedia 5 0
    Cognition Disorders Phenopedia 4 0
    Genomic Instability Phenopedia 4 0
    Mental Retardation Phenopedia 4 0
    Amenorrhea Phenopedia 3 0
    Aneuploidy Phenopedia 3 0
    Intelligence Tests Phenopedia 3 0
    Memory Phenopedia 3 0
    Reaction Time Phenopedia 3 0
    Executive Function Phenopedia 3 0
    Bipolar Disorder Phenopedia 2 0
    Cerebellar Ataxia Phenopedia 2 0
    Fibromyalgia Phenopedia 2 0
    Syndrome Phenopedia 2 0
    Polycystic Ovary Syndrome Phenopedia 2 0
    Attention Phenopedia 2 0
    Attention Deficit Disorder with Hyperactivity Phenopedia 2 0
    Memory, Short-Term Phenopedia 2 0
    Disease Progression Phenopedia 2 0
    Intellectual Disability Phenopedia 2 0
    Ovarian Diseases Phenopedia 2 0
    Abortion, Spontaneous Phenopedia 2 0
    Autoimmune Diseases Phenopedia 2 0
    Ovarian Neoplasms Phenopedia 2 0
    Essential Tremor Phenopedia 2 0
    Sex Chromosome Aberrations Phenopedia 2 0
    Mental Processes Phenopedia 2 0
    Migraine Disorders Phenopedia 1 0
    Olivopontocerebellar Atrophies Phenopedia 1 0
    Puberty, Delayed Phenopedia 1 0
    Spinocerebellar Ataxias Phenopedia 1 0
    Alzheimer Disease Phenopedia 1 0
    Dementia Phenopedia 1 0
    Ataxia Telangiectasia Phenopedia 1 0
    Mental Status Schedule Phenopedia 1 0
    Psychotic Disorders Phenopedia 1 0
    Puberty, Precocious Phenopedia 1 0
    Movement Disorders Phenopedia 1 0
    Tobacco Use Disorder Phenopedia 1 0
    Multiple Sclerosis Phenopedia 1 0
    Child Development Disorders, Pervasive Phenopedia 1 0
    Fetal Diseases Phenopedia 1 0
    Huntington Disease Phenopedia 1 0
    Mental Disorders Phenopedia 1 0
    Peripheral Nervous System Diseases Phenopedia 1 0
    Schizophrenic Psychology Phenopedia 1 0
    Trisomy Phenopedia 1 0
    Mood Disorders Phenopedia 1 0
    Multiple System Atrophy Phenopedia 1 0
    Obesity Phenopedia 1 0
    Breast Neoplasms Phenopedia 1 0
    Asymptomatic Diseases Phenopedia 1 0
    Space Perception Phenopedia 1 0
    Infertility Phenopedia 1 0
    Thrombophilia Phenopedia 1 0
    Hallucinations Phenopedia 1 0
    Inhibition (Psychology) Phenopedia 1 0
    Osteoporosis, Postmenopausal Phenopedia 1 0
    Adenocarcinoma Phenopedia 1 0
    Amyotrophic Lateral Sclerosis Phenopedia 1 0
    Neoplasms, Glandular and Epithelial Phenopedia 1 0
    Spinocerebellar Degenerations 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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