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224100
CDAN2
ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II
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Musculoskeletal Diseases
Joint Diseases
Arthritis
Gout
Rheumatic Diseases
Gout
Digestive System Diseases
Biliary Tract Diseases
Cholelithiasis
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Aplastic
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Dyserythropoietic, Congenital
Thalassemia
beta-Thalassemia
Anemia, Macrocytic
Bone Marrow Diseases
Anemia, Aplastic
Hemoglobinopathies
Thalassemia
beta-Thalassemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Dyserythropoietic, Congenital
Thalassemia
beta-Thalassemia
Hemoglobinopathies
Thalassemia
beta-Thalassemia
Metabolism, Inborn Errors
Hyperbilirubinemia, Hereditary
Gilbert Disease
Purine-Pyrimidine Metabolism, Inborn Errors
Gout
Nutritional and Metabolic Diseases
Metabolic Diseases
Iron Metabolism Disorders
Iron Overload
Metabolism, Inborn Errors
Hyperbilirubinemia, Hereditary
Gilbert Disease
Purine-Pyrimidine Metabolism, Inborn Errors
Gout
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Splenomegaly
Pathologic Processes
Disease Attributes
Disease Progression
Diseases in Twins
Hemolysis
Hyperbilirubinemia
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