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255310
CFTD
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION
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Musculoskeletal Diseases
Muscular Diseases
Muscle Weakness
Myopathies, Structural, Congenital
Myopathies, Nemaline
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Respiratory Tract Diseases
Respiration Disorders
Respiratory Insufficiency
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Seizures
Spinal Cord Diseases
Muscular Atrophy, Spinal
Nervous System Malformations
Neural Tube Defects
Neurodegenerative Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Neurologic Manifestations
Neurobehavioral Manifestations
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Seizures
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Muscular Diseases
Myopathies, Structural, Congenital
Myopathies, Nemaline
Peripheral Nervous System Diseases
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Cardiomyopathy, Dilated
Cardiomyopathies
Cardiomyopathy, Dilated
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Nervous System Malformations
Neural Tube Defects
Genetic Diseases, Inborn
Chromosome Disorders
Nutritional and Metabolic Diseases
Metabolic Diseases
Glucose Metabolism Disorders
Hyperinsulinism
Insulin Resistance
Endocrine System Diseases
Diabetes Mellitus
Diabetes Complications
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Growth Disorders
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Seizures
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