diagnosed using tool has mode of inheritance has causal genotype has causal or contributing genetic variation has manifestation has causal molecular phenotype in guideline Erythromycin Ischemic Cholitis Gastroenteritis Septic Arthritis Kidney Failure Focal Segmental Glomerulosclerosis Hypertension Delayed Puberty Cholelithiasis Hemiparesis Cirrhosis Intrahepatic Cholestasis Cardiac Failure Myocardial Infarction Splenomegaly Thrombocytopenia Neutropenia Hemolytic Anemia Megaloblastic Anemia Reticulocytopenia Anemia Leukocytosis Pneumonia Pulmonary Embolism Hepatomegaly Hyposthenuria Neonatal Hyperbilirubinemia Ventricular Tachycardia Chronic Hemolytic Anemia Hypovolemia Bronchiolitis Pyelonephritis Chronic Pain Mesangial Hypercellularity Cough Hepatic Vein Thrombosis Chest Pain Pulmonary Infiltrate Pulmonary Consolidation Intra-Abdominal Abscess Sickle Cell Disease-SS SCA SS and S/Beta-Zero Thalassemia Sickle Cell-SS Disease Severe SCD Sickle Cell Anemia SCDO:0000549 Homozygous Sickle Cell Disease Sickle Cell Hemoglobin S Disease A variant of sickle cell disease due to homozygosity of the E6V mutation, amino acid substitution of valine for glutamic acid in the sixth position of the beta chain, resulting in the production of hemoglobin S from both alleles. Hb SS-Disease Sufficient Hb SS Disease Sickle Cell Disease SS Hemoglobin SS Disease NCIT:C131682 Genetic Testing Hyperbilirubinemia Sickle Cell Dactylitis Cholecystitis Chronic Cholecystitis Acute Cholecystitis Ascending Cholangitis Osteonecrosis of the Femoral Head Urinary Tract Infection Posterior Reversible Leukoencephalopathy Blood Smear Acute Pancreatitis Glomerular Hypertrophy Renal Vein Thrombosis Spinal Cord Infarction Chronic Neuropathic Pain Hematuria Hemoglobin S Hemoglobin Profile Assay Leg Ulcer Pain Pulmonary Hypertension Sickle Retinopathy Acute Sickle Cell Crisis Vaso-Occlusive Crisis Renal Medullary Carcinoma Zinc Deficiency Splenic Infarction Hemolytic Crisis Chronic Hypersplenism Transient Ischemic Attack Angina Acute Hepatic Sequestration Functional Hyposplenism Chronic Anemia Hyperhemolysis Fever Gallbladder Empyema Acutely Severe Anemia Aplastic Crisis Hypersplenism Hyper-Hemolytic Crisis Acute Splenic Sequestration Crisis Acute Symptomatic Seizure Structural Hemoglobinopathy Right Upper Quadrant Syndrome Central Retinal Artery Occlusion Folate Deficiency Splenic Sequestration Renal Papillary Necrosis Abdominal Vaso-Occlusive Crisis HBB, GLU6VAL Hemoglobin Genotype SS Sickle Cell Disease Recommendations for the Management of Sickle Cell Disease in South Africa National Guideline for the Control and Management of Sickle Cell Disease Management of Sickle Cell Disease - The United Republic of Tanzania A Parental Guide to Managing Sickle Cell Disease Standards for Clinical Care of Adults with Sickle Cell Disease in the UK Sickle Cell Disease: The Clinical Care Guidelines of the Sickle Cell Unit Consensus Statement on the Care of Patients with Sickle Cell Disease in Canada Sickle Cell Disease in Children, Standards and Guidelines for Clinic Care Evidence-Based Management of Sickle Cell Disease Management of Children with Sickle Cell Disease in Europe: Current Situation and Future Perspectives ENERCA Clinical Recommendations for Disease Management and Prevention of Complications of Sickle Cell Disease in Children Autosomal Recessive Homozygous Osteonecrosis of the Humeral Head