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114240
CAPN3
CALPAIN 3
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Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophies, Limb-Girdle
Muscular Dystrophy, Duchenne
Myositis
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Dementia
Alzheimer Disease
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Spinal Cord Diseases
Muscular Atrophy, Spinal
Demyelinating Diseases
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Neurodegenerative Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Tauopathies
Alzheimer Disease
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophies, Limb-Girdle
Muscular Dystrophy, Duchenne
Myositis
Eye Diseases
Lens Diseases
Cataract
Hemic and Lymphatic Diseases
Hematologic Diseases
Leukocyte Disorders
Eosinophilia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Muscular Dystrophy, Duchenne
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis I
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Mucopolysaccharidoses
Mucopolysaccharidosis I
Muscular Dystrophies
Muscular Dystrophies, Limb-Girdle
Muscular Dystrophy, Duchenne
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis I
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 2
Lipid Metabolism Disorders
Lipidoses
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis I
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Mucopolysaccharidoses
Mucopolysaccharidosis I
Endocrine System Diseases
Diabetes Mellitus
Diabetes Mellitus, Type 2
Animal Diseases
Muscular Dystrophy, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Death
Cadaver
Postmortem Changes
Autolysis
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Signs and Symptoms
Body Weight
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