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Query OMIM entry list
191740
UGT1A1
UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A1
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Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Lymphoid
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Digestive System Diseases
Biliary Tract Diseases
Cholelithiasis
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Kernicterus
Male Urogenital Diseases
Urologic Diseases
Urination Disorders
Proteinuria
Hemoglobinuria
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Urination Disorders
Proteinuria
Hemoglobinuria
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Glucosephosphate Dehydrogenase Deficiency
Spherocytosis, Hereditary
Thalassemia
beta-Thalassemia
Blood Group Incompatibility
Erythroblastosis, Fetal
Kernicterus
Hemoglobinopathies
Anemia, Sickle Cell
Thalassemia
beta-Thalassemia
Leukocyte Disorders
Leukopenia
Agranulocytosis
Neutropenia
Lymphatic Diseases
Lymphoproliferative Disorders
Leukemia, Lymphoid
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Glucosephosphate Dehydrogenase Deficiency
Spherocytosis, Hereditary
Thalassemia
beta-Thalassemia
Hemoglobinopathies
Anemia, Sickle Cell
Thalassemia
beta-Thalassemia
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Hyperbilirubinemia, Hereditary
Crigler-Najjar Syndrome
Gilbert Disease
Infant, Newborn, Diseases
Erythroblastosis, Fetal
Kernicterus
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Kernicterus
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Hyperbilirubinemia, Hereditary
Crigler-Najjar Syndrome
Gilbert Disease
Immune System Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Kernicterus
Immunoproliferative Disorders
Lymphoproliferative Disorders
Leukemia, Lymphoid
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Nondisjunction, Genetic
Uniparental Disomy
Disease
Syndrome
Disease Attributes
Acute Disease
Hyperbilirubinemia
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal
Jaundice
Kernicterus
Signs and Symptoms
Skin Manifestations
Jaundice
Urological Manifestations
Proteinuria
Hemoglobinuria
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