Other laboratory abnormalities included thrombocytopenia, elevated D-dimer, abnormal liver enzymes, decreased albumin, low hemoglobin (Hb), elevated alkaline phosphate, eosinopenia, elevated uric acid, elevated ferritin, pancytopenia, prolonged activated partial thromboplastin time (APTT), low fibrinogen, and progressive coagulopathy. The gene discussed is GSTM1; the disease is blood coagulation disease.