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200150
CHAC
CHOREOACANTHOCYTOSIS
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Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Digestive System Diseases
Gastrointestinal Diseases
Esophageal Diseases
Deglutition Disorders
Otorhinolaryngologic Diseases
Pharyngeal Diseases
Deglutition Disorders
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Brain Diseases, Metabolic
Wernicke Encephalopathy
Dementia
Huntington Disease
Epilepsy
Epilepsies, Partial
Epilepsy, Temporal Lobe
Seizures
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Tic Disorders
Ocular Motility Disorders
Cranial Nerve Diseases
Ocular Motility Disorders
Demyelinating Diseases
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Huntington Disease
Parkinson Disease
Neurologic Manifestations
Dyskinesias
Ataxia
Athetosis
Chorea
Neuromuscular Manifestations
Muscular Atrophy
Seizures
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Ocular Motility Disorders
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Hemic and Lymphatic Diseases
Hematologic Diseases
Polycythemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Huntington Disease
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypobetalipoproteinemias
Abetalipoproteinemia
Muscular Dystrophies
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Vesiculobullous
Acantholysis
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Wernicke Encephalopathy
Lipid Metabolism Disorders
Dyslipidemias
Hypolipoproteinemias
Hypobetalipoproteinemias
Abetalipoproteinemia
Lipid Metabolism, Inborn Errors
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypobetalipoproteinemias
Abetalipoproteinemia
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin B Deficiency
Thiamine Deficiency
Wernicke Encephalopathy
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Acantholysis
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Chronic Disease
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Hemolysis
Signs and Symptoms
Body Weight
Body Weight Changes
Weight Loss
Neurologic Manifestations
Dyskinesias
Ataxia
Athetosis
Chorea
Neuromuscular Manifestations
Muscular Atrophy
Seizures
Substance-Related Disorders
Alcohol-Related Disorders
Wernicke Encephalopathy
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