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Query OMIM entry list
261650
PCK2
PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Digestive System Diseases
Liver Diseases
Hepatitis
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Cytochrome-c Oxidase Deficiency
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Infant, Newborn, Diseases
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Glucose Metabolism Disorders
Hypoglycemia
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Mitochondrial Myopathies
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Death
Death, Sudden
Sudden Infant Death
Signs and Symptoms
Failure to Thrive
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