2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of The Blood And Blood-Forming Organs 280-289 > Hereditary Hemolytic Anemias 282.* >  2008 ICD-9-CM Diagnosis 282.0
Hereditary spherocytosis- A familial congenital hemolytic anemia characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.
- Hemolytic anemia due to various intrinsic defects of the erythrocyte.
- 282.0 is a specific code that can be used to specify a diagnosis
- 282.0 contains 13 index entries
- View the ICD-9-CM Volume 1 282.* hierarchy
282.0 also known as:- Acholuric (familial) jaundice
- Congenital hemolytic anemia (spherocytic)
- Congenital spherocytosis
- Minkowski-Chauffard syndrome
- Spherocytosis (familial)
282.0 excludes:
Index entries containing 282.0:- Acholuric jaundice (familial) (splenomegalic) (see also Spherocytosis)
 282.0Anemia 285.9- congenital (following fetal blood loss) 776.5
- spherocytic (see also Spherocytosis) 282.0
- hemolytic 283.9
- congenital (spherocytic) (see also Spherocytosis) 282.0
- nonspherocytic - see Anemia, hemolytic, nonspherocytic, congenital
- spherocytic (hereditary) (see also Spherocytosis) 282.0
Disease, diseased - see also Syndrome- Holla (see also Spherocytosis) 282.0
Holla disease (see also Spherocytosis) 282.0
Icteroanemia, hemolytic (acquired) 283.9- congenital (see also Spherocytosis) 282.0
Icterus (see also Jaundice) 782.4- hemolytic (acquired) 283.9
- congenital (see also Spherocytosis) 282.0
Jaundice (yellow) 782.4- acholuric (familial) (splenomegalic) (see also Spherocytosis) 282.0
- hemolytic (acquired) 283.9
- congenital (see also Spherocytosis) 282.0
Minkowski-Chauffard syndrome (see also Spherocytosis) 282.0
Spherocytosis (congenital) (familial) (hereditary) 282.0Syndrome - see also Disease- Minkowski-Chauffard (see also Spherocytosis) 282.0
|
|
|
