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607839
GBE1
GLYCOGEN BRANCHING ENZYME
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Musculoskeletal Diseases
Muscular Diseases
Digestive System Diseases
Liver Diseases
Nervous System Diseases
Central Nervous System Diseases
Spinal Cord Diseases
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinal Muscular Atrophies of Childhood
Motor Neuron Disease
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Muscular Diseases
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Cardiomyopathy, Dilated
Cardiomyopathies
Cardiomyopathy, Dilated
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Genetic Diseases, Inborn
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Heredodegenerative Disorders, Nervous System
Spinal Muscular Atrophies of Childhood
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type IV
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type IV
Immune System Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Edema
Hydrops Fetalis
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
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