has clinical code has causal genotype has causal or contributing genetic variation has manifestation has causal molecular phenotype Hyposthenuria Isosthenuria Hemoglobin Trait D57.3 Sickle-cell trait Hematuria Sickle Cell Trait Hemoglobin Genotype AS http://purl.bioontology.org/ontology/MESH/D012805 The condition of being heterozygous for hemoglobin S. Sufficient SCDO:0001055 Haemoglobin Genotype AS AS Genotype MESH:D012805 Renal Medullary Carcinoma Splenic Infarction Adult Hemoglobin Renal Papillary Necrosis HBB, GLU6VAL Hemoglobin Genotype AS