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266120
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URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO
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Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Glucosephosphate Dehydrogenase Deficiency
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Glucosephosphate Dehydrogenase Deficiency
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Purine-Pyrimidine Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Purine-Pyrimidine Metabolism, Inborn Errors
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Substance-Related Disorders
Poisoning
Lead Poisoning
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