MeSH Treeview
Query OMIM entry list
610992
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PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY
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High-scoring List
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Database Center for Life Science
