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609286
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PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 3
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Ophthalmoplegia, Chronic Progressive External
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Parkinsonian Disorders
Movement Disorders
Parkinsonian Disorders
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Ophthalmoplegia, Chronic Progressive External
Eye Diseases
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Genital Diseases, Female
Adnexal Diseases
Ovarian Diseases
Menopause, Premature
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Mitochondrial Myopathies
Ophthalmoplegia, Chronic Progressive External
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease Attributes
Disease Progression
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
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