has clinical code diagnosed using tool has mode of inheritance has causal genotype has causal or contributing genetic variation has manifestation has causal molecular phenotype in guideline Severe Anemia Genetic Testing Blood Smear D57.2 Sickle-cell/Hb-C disease Hemoglobin C Hemoglobin S Hemoglobin Profile Assay Sickle Cell Disease-SC SCDO:0001059 MESH:D006450 Hemoglobin SC Disease SC Disease Sufficient Hb SC-disease http://purl.bioontology.org/ontology/MESH/D006450 Sickle Cell Disease SC One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia. Sickle-Cell/Hb-C Disease Sickle Cell Hemoglobin C Disease Sickle Cell-Haemoglobin C Disease Hemoglobin S / Hemoglobin C Disease Sickle Cell-Hemoglobin C Disease Structural Hemoglobinopathy HBB, GLU6VAL HBB, GLU6LYS Hemoglobin Genotype SC 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 ENERCA Clinical Recommendations for Disease Management and Prevention of Complications of Sickle Cell Disease in Children Compound Heterozygous Sickle Cell Disease Autosomal Recessive Compound Heterozygous