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138320
GPX1
GLUTATHIONE PEROXIDASE
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Bacterial Infections and Mycoses
Infection
Urinary Tract Infections
Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Leukemia, Promyelocytic, Acute
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Down Syndrome
Eye Diseases
Eye Diseases, Hereditary
Albinism
Lens Diseases
Cataract
Male Urogenital Diseases
Urologic Diseases
Urinary Tract Infections
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Urinary Tract Infections
Cardiovascular Diseases
Heart Diseases
Cardiac Output, Low
Myocardial Ischemia
Coronary Disease
Coronary Artery Disease
Myocardial Infarction
Ventricular Dysfunction
Ventricular Dysfunction, Left
Vascular Diseases
Arterial Occlusive Diseases
Arteriosclerosis
Coronary Artery Disease
Myocardial Ischemia
Coronary Disease
Coronary Artery Disease
Myocardial Infarction
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Glucosephosphate Dehydrogenase Deficiency
Methemoglobinemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Down Syndrome
Chromosome Disorders
Down Syndrome
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Glucosephosphate Dehydrogenase Deficiency
Chromosome Disorders
Down Syndrome
Eye Diseases, Hereditary
Albinism
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Skin Diseases, Genetic
Albinism
Infant, Newborn, Diseases
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal
Skin and Connective Tissue Diseases
Skin Diseases
Hair Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Skin Diseases, Genetic
Albinism
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Trisomy
Chromosome Duplication
Trisomy
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Hemolysis
Hyperbilirubinemia
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal
Signs and Symptoms
Cardiac Output, Low
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