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258450
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PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Digestive System Diseases
Gastrointestinal Diseases
Esophageal Diseases
Deglutition Disorders
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Pharyngeal Diseases
Deglutition Disorders
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Parkinsonian Disorders
Parkinson Disease
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
Cerebellar Diseases
Cerebellar Ataxia
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Movement Disorders
Parkinsonian Disorders
Parkinson Disease
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Neurodegenerative Diseases
Parkinson Disease
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Dystonia
Tremor
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Reflex, Abnormal
Sensation Disorders
Hearing Disorders
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Eye Diseases
Eyelid Diseases
Blepharoptosis
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Kearns-Sayre Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Genital Diseases, Female
Adnexal Diseases
Ovarian Diseases
Menopause, Premature
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Cardiomyopathy, Dilated
Cardiomyopathies
Cardiomyopathy, Dilated
Kearns-Sayre Syndrome
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
Cytochrome-c Oxidase Deficiency
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Kearns-Sayre Syndrome
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Endocrine System Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Inflammation
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Dystonia
Tremor
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Reflex, Abnormal
Sensation Disorders
Hearing Disorders
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