2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > Hereditary Hemolytic Anemias 282.* > 2006 ICD-9-CM Diagnosis 282.60 Sickle-cell disease unspecified View the most recent version of ICD-9-CM 282.60 A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. 282.60 is a specific code that can be used to specify a diagnosis 282.60 contains 13 index entries View the ICD-9-CM Volume 1 282.* hierarchy Alternate Terminology Sickle-cell anemia NOS  Index entries containing 282.60: Anemia 285.9 drepanocytic (see also Disease, sickle-cell) 282.60 sickle-cell (see also Disease, sickle-cell) 282.60 Disease, diseased - see also Syndrome sickle-cell 282.60 with crisis 282.62 Hb-S disease 282.61 other abnormal hemoglobin (Hb-D) (Hb-E) (Hb-G) (Hb-J) (Hb-K) (Hb-O) (Hb-P) (high fetal gene) (without crisis) 282.68 with crisis 282.69 elliptocytosis 282.60 Hb-C (without crisis) 282.63 with crisis 282.64 vaso-occlusive pain 282.64 Hb-S 282.61 with crisis 282.62 Hb-C (without crisis) 282.63 with crisis 282.64 vaso-occlusive pain 282.64 other abnormal hemoglobin (Hb-D) (Hb-E) (Hb-G) (Hb-J) (Hb-K) (Hb-O) (Hb-P) (high fetal gene) (without crisis) 282.68 with crisis 282.69 spherocytosis 282.60 thalassemia (without crisis) 282.41 with crisis 282.42 vaso-occlusive pain 282.42 Drepanocytic anemia (see also Disease, sickle cell) 282.60 Elliptocytosis (congenital) (hereditary) 282.1 sickle-cell (disease) 282.60 trait 282.5 Hemoglobinopathy (mixed) (see also Disease, hemoglobin) 282.7 sickle-cell 282.60 with thalassemia (without crisis) 282.41 with crisis 282.42 vaso-occlusive pain 282.42 Meniscocytosis 282.60 Sickle-cell anemia (see also Disease, sickle-cell) 282.60 disease (see also Disease, sickle-cell) 282.60 Sicklemia (see also Disease, sickle-cell) 282.60 trait 282.5 Spherocytosis (congenital) (familial) (hereditary) 282.0 sickle-cell (disease) 282.60