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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 282.1 Hereditary elliptocytosis  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 Therefore, this code may be out of date.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 282.1 can be accessed here. An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape. 282.1 is a specific code that can be used to specify a diagnosis 282.1 contains 8 index entries View the ICD-9-CM Volume 1 282.* hierarchy 282.1 also known as: Elliptocytosis (congenital) Ovalocytosis (congenital) (hereditary) Index entries containing 282.1: Anemia 285.9 elliptocytosis (see also Elliptocytosis) 282.1 hemolytic 283.9 elliptocytotic (see also Elliptocytosis) 282.1 ovalocytosis (hereditary) (see also Elliptocytosis) 282.1 Dresbach's syndrome (elliptocytosis) 282.1 Elliptocytosis (congenital) (hereditary) 282.1 Hb-C (disease) 282.7 hemoglobin disease 282.7 sickle-cell (disease) 282.60 trait 282.5 Erythrocytosis (megalosplenic) oval, hereditary (see also Elliptocytosis) 282.1 Ovalocytosis (congenital) (hereditary) (see also Elliptocytosis) 282.1 Syndrome - see also Disease Dresbach's (elliptocytosis) 282.1