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236270
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HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN METABOLISM, cblE COMPLEMENTATION TYPE
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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
Homocystinuria
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Macrocytic
Anemia, Megaloblastic
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
Amino Acid Metabolism, Inborn Errors
Hyperhomocysteinemia
Homocystinuria
Brain Diseases, Metabolic, Inborn
Homocystinuria
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Homocystinuria
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Homocystinuria
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Hyperhomocysteinemia
Homocystinuria
Brain Diseases, Metabolic, Inborn
Homocystinuria
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin B Deficiency
Vitamin B 12 Deficiency
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Failure to Thrive
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
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