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310400
MTM1
MYOTUBULAR MYOPATHY 1
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Musculoskeletal Diseases
Muscular Diseases
Muscle Weakness
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myopathies, Structural, Congenital
Myotonic Disorders
Myotonia Congenita
Myotonic Dystrophy
Digestive System Diseases
Digestive System Abnormalities
Diaphragmatic Eventration
Gastrointestinal Diseases
Liver Diseases
Zellweger Syndrome
Respiratory Tract Diseases
Lung Diseases
Respiratory Distress Syndrome, Newborn
Respiration Disorders
Respiratory Distress Syndrome, Newborn
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Peroxisomal Disorders
Zellweger Syndrome
Hydrocephalus
Intracranial Hypertension
Hydrocephalus
Spinal Cord Diseases
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Myotonia Congenita
Myotonic Dystrophy
Spinal Muscular Atrophies of Childhood
Motor Neuron Disease
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Mucopolysaccharidosis II
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Muscular Atrophy
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myopathies, Structural, Congenital
Myotonic Disorders
Myotonia Congenita
Myotonic Dystrophy
Peripheral Nervous System Diseases
Eye Diseases
Eye Abnormalities
Eyelid Diseases
Blepharoptosis
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Zellweger Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Zellweger Syndrome
Pregnancy Complications
Fetal Diseases
Hemic and Lymphatic Diseases
Hematologic Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Zellweger Syndrome
Chromosome Disorders
Digestive System Abnormalities
Diaphragmatic Eventration
Eye Abnormalities
Fetal Diseases
Genetic Diseases, Inborn
Chromosome Disorders
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Mucopolysaccharidosis II
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Mucopolysaccharidosis II
Myotonia Congenita
Myotonic Dystrophy
Spinal Muscular Atrophies of Childhood
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Peroxisomal Disorders
Zellweger Syndrome
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type II
Mucopolysaccharidoses
Mucopolysaccharidosis II
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Mucopolysaccharidoses
Mucopolysaccharidosis II
Peroxisomal Disorders
Zellweger Syndrome
Muscular Dystrophies
Myotonic Dystrophy
Infant, Newborn, Diseases
Asphyxia Neonatorum
Infant, Premature, Diseases
Respiratory Distress Syndrome, Newborn
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis II
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Peroxisomal Disorders
Zellweger Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Peroxisomal Disorders
Zellweger Syndrome
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type II
Mucopolysaccharidoses
Mucopolysaccharidosis II
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Mucopolysaccharidoses
Mucopolysaccharidosis II
Peroxisomal Disorders
Zellweger Syndrome
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Hypertrophy
Pathologic Processes
Chromosome Aberrations
Sex Chromosome Aberrations
Translocation, Genetic
Death
Asphyxia
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Muscle Weakness
Signs and Symptoms
Body Weight
Birth Weight
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Muscular Atrophy
Wounds and Injuries
Asphyxia
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