MeSH Treeview
Query OMIM entry list
606434
UGT1A9
UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A9
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Digestive System Diseases
Liver Diseases
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Parkinsonian Disorders
Parkinson Disease
Movement Disorders
Parkinsonian Disorders
Parkinson Disease
Neurodegenerative Diseases
Parkinson Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Hyperbilirubinemia, Hereditary
Crigler-Najjar Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Hyperbilirubinemia, Hereditary
Crigler-Najjar Syndrome
Database Center for Life Science
