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141800
HBA1
HEMOGLOBIN--ALPHA LOCUS 1
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Bacterial Infections and Mycoses
Infection
Communicable Diseases
Parasitic Diseases
Protozoan Infections
Malaria
Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Experimental
Leukemia, Lymphoid
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Leukemia, Erythroblastic, Acute
Neoplasms, Experimental
Leukemia, Experimental
Digestive System Diseases
Liver Diseases
Hepatomegaly
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebrovascular Disorders
Male Urogenital Diseases
Genital Diseases, Male
Penile Diseases
Hypospadias
Urogenital Abnormalities
Hypospadias
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Hypospadias
Pregnancy Complications
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Pregnancy Complications, Hematologic
Cardiovascular Diseases
Heart Diseases
Myocardial Ischemia
Myocardial Infarction
Vascular Diseases
Cerebrovascular Disorders
Hypotension
Myocardial Ischemia
Myocardial Infarction
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Sickle Cell
Sickle Cell Trait
Glucosephosphate Dehydrogenase Deficiency
Favism
Thalassemia
alpha-Thalassemia
beta-Thalassemia
Favism
Hemoglobinuria, Paroxysmal
Anemia, Hypochromic
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Bone Marrow Diseases
Myelodysplastic Syndromes
Hemoglobinuria, Paroxysmal
Myeloproliferative Disorders
Leukemia, Erythroblastic, Acute
Polycythemia Vera
Hemoglobinopathies
Anemia, Sickle Cell
Sickle Cell Trait
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
beta-Thalassemia
Methemoglobinemia
Polycythemia
Pregnancy Complications, Hematologic
Lymphatic Diseases
Lymphoproliferative Disorders
Leukemia, Lymphoid
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Urogenital Abnormalities
Hypospadias
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Sickle Cell
Sickle Cell Trait
Glucosephosphate Dehydrogenase Deficiency
Favism
Thalassemia
alpha-Thalassemia
beta-Thalassemia
Chromosome Disorders
Hemoglobinopathies
Anemia, Sickle Cell
Sickle Cell Trait
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
beta-Thalassemia
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Infant, Newborn, Diseases
Nutritional and Metabolic Diseases
Metabolic Diseases
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Endocrine System Diseases
Diabetes Mellitus
Diabetes Complications
Diabetic Coma
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Immune System Diseases
Autoimmune Diseases
Diabetes Mellitus, Type 1
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Hypersensitivity
Immunoproliferative Disorders
Lymphoproliferative Disorders
Leukemia, Lymphoid
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Hepatomegaly
Splenomegaly
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Diseases in Twins
Hemolysis
Hyperbilirubinemia
Jaundice
Signs and Symptoms
Cyanosis
Edema
Hydrops Fetalis
Fatigue
Skin Manifestations
Jaundice
Substance-Related Disorders
Poisoning
Foodborne Diseases
Favism
Plant Poisoning
Favism
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