diagnosed using tool has mode of inheritance has causal genotype has causal or contributing genetic variation has causal molecular phenotype Sickle Cell Disease-SD Genetic Testing Blood Smear Hemoglobin S Hemoglobin D-Punjab Hemoglobin Profile Assay Sickle Cell Disease-S/D-Punjab A rare compound heterozygous hemoglobinopathy characterised by the presence of two beta globin gene variants: that of hemoglobin S (beta-6(GAG-->GTG)) and that of hemoglobin D-Punjab (beta-121(GAA-->CAA)). Request inclusion into relevant ontology. Perhaps as sub-class of "Sickle Cell-Hemoglobin D Disease" in the NCIT. Rahimah Ahmad*, Syahira Lazira Omar*, Siti Hida H M Arif*, Faidatul Syazlin A Hamid*, Nur Aisyah Aziz*, Nik Hafidzah N Mustapha**, Zubaidah Zakaria*Haemoglobin Sickle D Punjab: - A Case Report. Med J Malaysia. 2014. Vol 69 No 1. Sickle Cell-Haemoglobin D-Punjab Few but definitions not freely available Sickle Cell-Hemoglobin D-Punjab Disease Hemoglobin S/D-Punjab Haemoglobin S/D-Punjab HBB, GLU6VAL Hemoglobin Genotype S/D-Punjab HBB, GLU121GLN Autosomal Recessive Compound Heterozygous