2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > Hereditary Hemolytic Anemias 282.* >
 2007 ICD-9-CM Diagnosis 282.60
Sickle-cell disease unspecified On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date.
The 2009 version of ICD-9-CM 282.60 can be accessed here. - 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
282.60 also known as:
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
- elliptocytosis 282.60
- Hb-C (without crisis) 282.63
- Hb-S 282.61
- with
- other abnormal hemoglobin (Hb-D) (Hb-E) (Hb-G) (Hb-J) (Hb-K) (Hb-O) (Hb-P) (high fetal gene) (without crisis) 282.68
- spherocytosis 282.60
- thalassemia (without crisis) 282.41
Drepanocytic anemia (see also Disease, sickle cell) 282.60
Elliptocytosis (congenital) (hereditary) 282.1- sickle-cell (disease) 282.60
Hemoglobinopathy (mixed) (see also Disease, hemoglobin) 282.7- sickle-cell 282.60
- with thalassemia (without crisis) 282.41
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) 282.60Spherocytosis (congenital) (familial) (hereditary) 282.0- sickle-cell (disease) 282.60
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