MeSH Treeview
Query OMIM entry list
608799
CDG1E
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Epilepsy
Seizures
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurologic Manifestations
Seizures
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Carbohydrate Metabolism, Inborn Errors
Congenital Disorders of Glycosylation
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Carbohydrate Metabolism, Inborn Errors
Congenital Disorders of Glycosylation
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Seizures
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