MeSH Treeview
Query OMIM entry list
607143
CDG1G
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig
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Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypertonia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypertonia
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