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182900
HS
SPHEROCYTOSIS, HEREDITARY
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Virus Diseases
DNA Virus Infections
Parvoviridae Infections
RNA Virus Infections
Orthomyxoviridae Infections
Influenza, Human
Musculoskeletal Diseases
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Digestive System Diseases
Biliary Tract Diseases
Cholelithiasis
Gallbladder Diseases
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Mouth Diseases
Lip Diseases
Cleft Lip
Mouth Abnormalities
Cleft Lip
Cleft Palate
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Mouth Abnormalities
Cleft Lip
Cleft Palate
Respiratory Tract Diseases
Respiratory Tract Infections
Influenza, Human
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Kidney Diseases, Cystic
Polycystic Kidney Diseases
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Kidney Diseases, Cystic
Polycystic Kidney Diseases
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Aplastic
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Elliptocytosis, Hereditary
Spherocytosis, Hereditary
Thalassemia
Blood Protein Disorders
Bone Marrow Diseases
Anemia, Aplastic
Hemoglobinopathies
Anemia, Sickle Cell
Thalassemia
Pancytopenia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Mouth Abnormalities
Cleft Lip
Cleft Palate
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Elliptocytosis, Hereditary
Spherocytosis, Hereditary
Thalassemia
Chromosome Disorders
Hemoglobinopathies
Anemia, Sickle Cell
Thalassemia
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Hyperbilirubinemia, Hereditary
Gilbert Disease
Metal Metabolism, Inborn Errors
Hemochromatosis
Infant, Newborn, Diseases
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal
Nutritional and Metabolic Diseases
Metabolic Diseases
Iron Metabolism Disorders
Iron Overload
Hemochromatosis
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Hyperbilirubinemia, Hereditary
Gilbert Disease
Metal Metabolism, Inborn Errors
Hemochromatosis
Endocrine System Diseases
Gonadal Disorders
Hypogonadism
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Splenomegaly
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease Attributes
Acute Disease
Hemolysis
Hyperbilirubinemia
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal
Jaundice
Signs and Symptoms
Skin Manifestations
Jaundice
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