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253600
LGMD2A
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A
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Musculoskeletal Diseases
Joint Diseases
Contracture
Muscular Diseases
Contracture
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophies, Limb-Girdle
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
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Demyelinating Diseases
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophies, Limb-Girdle
Myositis
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Heart Arrest
Hemic and Lymphatic Diseases
Hematologic Diseases
Leukocyte Disorders
Eosinophilia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
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
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
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
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Signs and Symptoms
Body Weight
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
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