The most common abnormalities shown in the laboratory results that were elevated C-reactive protein (CRP) (94.23%), elevated D-dimer (90.63%), elevated interleukin 6 (IL-6) (88.46%), elevated fibrinogen (88%), hypoproteinemia (66.67%), decreased vitamin D (62.22%), elevated lactate dehydrogenase (LDH) (56%), hyperglycemia (48.78%), anemia (48.08%), elevated alkaline phosphatase (ALP) (46.15%), elevated aspartate aminotransferase (AST) (40.38%), lymphopenia (38.46%), neutrophilia (30.77%), elevated alanine transaminase (ALT) (30%), and elevated bile acids (35.71%). The gene discussed is GPT; the disease is anemia (phenotype).