MeSH Treeview
Query OMIM entry list
141900
HBB
HEMOGLOBIN--BETA LOCUS
→
High-scoring List
Bacterial Infections and Mycoses
Bacterial Infections
Gram-Negative Bacterial Infections
Enterobacteriaceae Infections
Proteus Infections
Gram-Positive Bacterial Infections
Streptococcal Infections
Pneumococcal Infections
Infection
Sepsis
Urinary Tract Infections
Virus Diseases
DNA Virus Infections
Parvoviridae Infections
Erythema Infectiosum
Hepatitis, Viral, Human
Skin Diseases, Viral
Erythema Infectiosum
Parasitic Diseases
Parasitemia
Protozoan Infections
Malaria
Malaria, Falciparum
Neoplasms
Hamartoma
Hamartoma Syndrome, Multiple
Neoplasms by Histologic Type
Leukemia
Leukemia, Lymphoid
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Leukemia, Erythroblastic, Acute
Neoplasms, Glandular and Epithelial
Carcinoma
Carcinoma, Small Cell
Neoplasms by Site
Thoracic Neoplasms
Respiratory Tract Neoplasms
Lung Neoplasms
Neoplasms, Multiple Primary
Hamartoma Syndrome, Multiple
Neoplastic Processes
Neoplasm Metastasis
Neoplastic Syndromes, Hereditary
Hamartoma Syndrome, Multiple
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Metabolic
Osteomalacia
Digestive System Diseases
Biliary Tract Diseases
Cholelithiasis
Liver Diseases
Hepatitis
Hepatitis, Viral, Human
Hepatomegaly
Liver Cirrhosis
Pancreatic Diseases
Cystic Fibrosis
Pancreatitis
Respiratory Tract Diseases
Lung Diseases
Cystic Fibrosis
Hypertension, Pulmonary
Lung Neoplasms
Pulmonary Fibrosis
Respiratory Tract Neoplasms
Lung Neoplasms
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Neurologic Manifestations
Pain
Neuralgia
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Neuromuscular Diseases
Peripheral Nervous System Diseases
Neuralgia
Eye Diseases
Eye Manifestations
Retinal Diseases
Male Urogenital Diseases
Genital Diseases, Male
Penile Diseases
Priapism
Urologic Diseases
Kidney Diseases
Kidney Papillary Necrosis
Uremia
Hemolytic-Uremic Syndrome
Urinary Tract Infections
Urination Disorders
Hematuria
Proteinuria
Hemoglobinuria
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Kidney Papillary Necrosis
Uremia
Hemolytic-Uremic Syndrome
Urinary Tract Infections
Urination Disorders
Hematuria
Proteinuria
Hemoglobinuria
Pregnancy Complications
Fetal Diseases
Erythroblastosis, Fetal
Pregnancy Complications, Hematologic
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Vascular Diseases
Embolism and Thrombosis
Thromboembolism
Thrombosis
Thromboembolism
Hypertension
Splenic Infarction
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Aplastic
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Sickle Cell
Hemoglobin SC Disease
Sickle Cell Trait
Glucosephosphate Dehydrogenase Deficiency
Hemoglobin C Disease
Spherocytosis, Hereditary
Thalassemia
alpha-Thalassemia
beta-Thalassemia
Hemolytic-Uremic Syndrome
Anemia, Hypochromic
Anemia, Macrocytic
Blood Group Incompatibility
Erythroblastosis, Fetal
Rh Isoimmunization
Blood Platelet Disorders
Thrombocytopenia
Thrombotic Microangiopathies
Hemolytic-Uremic Syndrome
Bone Marrow Diseases
Anemia, Aplastic
Myeloproliferative Disorders
Leukemia, Erythroblastic, Acute
Polycythemia Vera
Hemoglobinopathies
Anemia, Sickle Cell
Hemoglobin SC Disease
Sickle Cell Trait
Hemoglobin C Disease
Thalassemia
alpha-Thalassemia
beta-Thalassemia
Leukocyte Disorders
Leukopenia
Agranulocytosis
Methemoglobinemia
Polycythemia
Pregnancy Complications, Hematologic
Lymphatic Diseases
Lymphoproliferative Disorders
Leukemia, Lymphoid
Splenic Diseases
Hypersplenism
Splenic Infarction
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Fetal Diseases
Erythroblastosis, Fetal
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Sickle Cell
Hemoglobin SC Disease
Sickle Cell Trait
Glucosephosphate Dehydrogenase Deficiency
Hemoglobin C Disease
Spherocytosis, Hereditary
Thalassemia
alpha-Thalassemia
beta-Thalassemia
Chromosome Disorders
Cystic Fibrosis
Hemoglobinopathies
Anemia, Sickle Cell
Hemoglobin SC Disease
Sickle Cell Trait
Hemoglobin C Disease
Thalassemia
alpha-Thalassemia
beta-Thalassemia
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Hyperbilirubinemia, Hereditary
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypobetalipoproteinemias
Abetalipoproteinemia
Metal Metabolism, Inborn Errors
Hemochromatosis
Neoplastic Syndromes, Hereditary
Hamartoma Syndrome, Multiple
Infant, Newborn, Diseases
Cystic Fibrosis
Erythroblastosis, Fetal
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal
Skin and Connective Tissue Diseases
Skin Diseases
Erythema
Erythema Infectiosum
Skin Diseases, Infectious
Skin Diseases, Viral
Erythema Infectiosum
Skin Ulcer
Leg Ulcer
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Osteomalacia
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Iron Metabolism Disorders
Iron Overload
Hemochromatosis
Lipid Metabolism Disorders
Dyslipidemias
Hypolipoproteinemias
Hypobetalipoproteinemias
Abetalipoproteinemia
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Hyperbilirubinemia, Hereditary
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypobetalipoproteinemias
Abetalipoproteinemia
Metal Metabolism, Inborn Errors
Hemochromatosis
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin D Deficiency
Osteomalacia
Endocrine System Diseases
Diabetes Mellitus
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Immune System Diseases
Autoimmune Diseases
Diabetes Mellitus, Type 1
Blood Group Incompatibility
Erythroblastosis, Fetal
Rh Isoimmunization
Immunoproliferative Disorders
Lymphoproliferative Disorders
Leukemia, Lymphoid
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Cardiomegaly
Hepatomegaly
Splenomegaly
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Inversion
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Acute Disease
Chronic Disease
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Recurrence
Growth Disorders
Hemolysis
Hemorrhage
Hematuria
Hyperbilirubinemia
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal
Jaundice
Hyperplasia
Inflammation
Systemic Inflammatory Response Syndrome
Sepsis
Parasitemia
Neoplastic Processes
Neoplasm Metastasis
Postoperative Complications
Signs and Symptoms
Body Temperature Changes
Fever
Cyanosis
Eye Manifestations
Fatigue
Neurologic Manifestations
Pain
Neuralgia
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Pain
Chest Pain
Neuralgia
Signs and Symptoms, Respiratory
Anoxia
Hypercapnia
Skin Manifestations
Jaundice
Urological Manifestations
Proteinuria
Hemoglobinuria
Database Center for Life Science
