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Genopedia


TRNL1

67 disease terms (MeSH) has been reported with TRNL1 gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Diabetes Mellitus, Type 2 Phenopedia 16 0
    Mitochondrial Diseases Phenopedia 13 0
    MELAS Syndrome Phenopedia 11 1
    Hearing Loss, Sensorineural Phenopedia 10 0
    Diabetes Mellitus Phenopedia 10 0
    Hearing Loss Phenopedia 8 0
    Deafness Phenopedia 6 0
    Diabetes Mellitus, Type 1 Phenopedia 5 0
    Mitochondrial Encephalomyopathies Phenopedia 5 0
    Diabetes Complications Phenopedia 4 0
    Diabetic Neuropathies Phenopedia 3 0
    Diabetic Ketoacidosis Phenopedia 2 0
    MERRF Syndrome Phenopedia 2 0
    Hypertrophy, Left Ventricular Phenopedia 2 0
    Insulin Resistance Phenopedia 2 0
    Intestinal Pseudo-Obstruction Phenopedia 2 0
    Kearns-Sayer Syndrome Phenopedia 2 0
    Spinocerebellar Ataxias Phenopedia 2 0
    Spinocerebellar Degenerations Phenopedia 1 0
    Stroke Phenopedia 1 0
    Werner Syndrome Phenopedia 1 0
    Wolff-Parkinson-White Syndrome Phenopedia 1 0
    Learning Disorders Phenopedia 1 0
    Leigh Disease Phenopedia 1 0
    Lung Neoplasms Phenopedia 1 1
    Migraine Disorders Phenopedia 1 0
    Mitochondrial Myopathies Phenopedia 1 0
    Motor Neuron Disease Phenopedia 1 0
    Muscle Hypotonia Phenopedia 1 0
    Muscular Diseases Phenopedia 1 0
    Muscular Dystrophies Phenopedia 1 0
    Myocardial Infarction Phenopedia 1 0
    Obesity Phenopedia 1 0
    Pancreatitis Phenopedia 1 0
    Parkinson Disease Phenopedia 1 0
    Plaque, Atherosclerotic Phenopedia 1 0
    Recurrence Phenopedia 1 0
    Retinal Dystrophies Phenopedia 1 0
    Sick Sinus Syndrome Phenopedia 1 0
    Diabetic Nephropathies Phenopedia 1 0
    Glucose Intolerance Phenopedia 1 0
    Hearing Disorders Phenopedia 1 0
    Heart Diseases Phenopedia 1 0
    Hyperglycemia Phenopedia 1 0
    Hypertension Phenopedia 1 0
    Diabetic Retinopathy Phenopedia 1 0
    Disease Phenopedia 1 0
    Endometrial Neoplasms Phenopedia 1 0
    Gait Disorders, Neurologic Phenopedia 1 0
    Genetic Diseases, Inborn Phenopedia 1 0
    Demyelinating Diseases Phenopedia 1 0
    Alzheimer Disease Phenopedia 1 0
    Aortic Diseases Phenopedia 1 0
    Arrhythmia Phenopedia 1 0
    Ataxia Phenopedia 1 0
    Atherosclerosis Phenopedia 1 0
    Atrophy Phenopedia 1 0
    Autoimmune Diseases Phenopedia 1 0
    Body Weight Phenopedia 1 0
    Cardiomyopathies Phenopedia 1 0
    Cardiovascular Diseases Phenopedia 1 0
    Carotid Artery Diseases Phenopedia 1 0
    Cerebrovascular Accident Phenopedia 1 1
    Child Development Disorders, Pervasive Phenopedia 1 0
    Chronic Disease Phenopedia 1 0
    Coronary Artery Disease Phenopedia 1 0
    Cytochrome-c Oxidase Deficiency 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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