MeSH Treeview
Query OMIM entry list
232050
PCCB
PROPIONYL-CoA CARBOXYLASE, BETA SUBUNIT
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Carboxylase Deficiency Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Carboxylase Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Carboxylase Deficiency Disease
Mitochondrial Diseases
Pyruvate Carboxylase Deficiency Disease
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Database Center for Life Science
