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238970
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HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME
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Digestive System Diseases
Liver Diseases
Respiratory Tract Diseases
Lung Diseases
Respiratory Distress Syndrome, Newborn
Hyaline Membrane Disease
Respiration Disorders
Respiratory Distress Syndrome, Newborn
Hyaline Membrane Disease
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
Citrullinemia
Epilepsy
Seizures
Neurologic Manifestations
Dyskinesias
Ataxia
Myoclonus
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Paresis
Paraparesis
Paraparesis, Spastic
Seizures
Eye Diseases
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Urea Cycle Disorders, Inborn
Citrullinemia
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
Citrullinemia
Infant, Newborn, Diseases
Infant, Premature, Diseases
Respiratory Distress Syndrome, Newborn
Hyaline Membrane Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
Citrullinemia
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Urea Cycle Disorders, Inborn
Citrullinemia
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
Citrullinemia
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Disease Attributes
Recurrence
Hyperammonemia
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Myoclonus
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Paresis
Paraparesis
Paraparesis, Spastic
Seizures
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