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208920
EAOH
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
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Musculoskeletal Diseases
Muscular Diseases
Muscle Weakness
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Ataxia Telangiectasia
Spinocerebellar Degenerations
Friedreich Ataxia
Myoclonic Cerebellar Dyssynergia
Spinocerebellar Ataxias
Dementia
Epilepsy
Seizures
Movement Disorders
Ocular Motility Disorders
Spinal Cord Diseases
Spinocerebellar Degenerations
Friedreich Ataxia
Myoclonic Cerebellar Dyssynergia
Spinocerebellar Ataxias
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Oculomotor Nerve Diseases
Ophthalmoplegia
Oculomotor Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Demyelinating Diseases
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurocutaneous Syndromes
Ataxia Telangiectasia
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Spinocerebellar Degenerations
Friedreich Ataxia
Myoclonic Cerebellar Dyssynergia
Spinocerebellar Ataxias
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Ataxia Telangiectasia
Dystonia
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Apraxias
Neuromuscular Manifestations
Fasciculation
Muscle Weakness
Paralysis
Ophthalmoplegia
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Eye Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Oculomotor Nerve Diseases
Ophthalmoplegia
Optic Nerve Diseases
Optic Atrophy
Cardiovascular Diseases
Vascular Diseases
Telangiectasis
Ataxia Telangiectasia
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Protein Disorders
Hypoproteinemia
Hypoalbuminemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Ataxia Telangiectasia
Chromosome Disorders
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Spinocerebellar Degenerations
Friedreich Ataxia
Myoclonic Cerebellar Dyssynergia
Spinocerebellar Ataxias
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipoproteinemia Type II
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Ataxia Telangiectasia
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hyperlipoproteinemias
Hyperlipoproteinemia Type II
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipoproteinemia Type II
Mitochondrial Diseases
Friedreich Ataxia
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin E Deficiency
Immune System Diseases
Immunologic Deficiency Syndromes
Ataxia Telangiectasia
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Progression
Muscle Weakness
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Dystonia
Neurobehavioral Manifestations
Apraxias
Intellectual Disability
Psychomotor Disorders
Apraxias
Neuromuscular Manifestations
Fasciculation
Muscle Weakness
Paralysis
Ophthalmoplegia
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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