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 282.7 Other hemoglobinopathies View the most recent version of ICD-9-CM 282.7 Hemoglobins characterized by structural alterations within the molecule. The alteration can be either absence, addition or substitution of one or more amino acids in the globin part of the molecule at selected positions in the polypeptide chains. A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice. A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. 282.7 is a specific code that can be used to specify a diagnosis 282.7 contains 38 index entries View the ICD-9-CM Volume 1 282.* hierarchy Alternate Terminology Abnormal hemoglobin NOS Congenital Heinz-body anemia Disease: hemoglobin C [Hb-C] hemoglobin D [Hb-D] hemoglobin E [Hb-E] hemoglobin Zurich [Hb-Zurich] Hemoglobinopathy NOS Hereditary persistence of fetal hemoglobin [HPFH] Unstable hemoglobin hemolytic disease 282.7 Excludes familial polycythemia (289.6) hemoglobin M [Hb-M] disease (289.7) high-oxygen-affinity hemoglobin (289.0)  Index entries containing 282.7: Abnormal, abnormality, abnormalities - see also Anomaly hemoglobin (see also Disease, hemoglobin) 282.7 trait - see Trait, hemoglobin, abnormal Anemia 285.9 congenital (following fetal blood loss) 776.5 Heinz-body 282.7 Heinz-body, congenital 282.7 hemolytic 283.9 Stransky-Regala type (Hb-E) (see also Disease, hemoglobin) 282.7 Disease, diseased - see also Syndrome hemoglobin (Hb) 282.7 with thalassemia 282.49 abnormal (mixed) NEC 282.7 with thalassemia 282.49 AS genotype 282.5 Bart's 282.49 C (Hb-C) 282.7 with other abnormal hemoglobin NEC 282.7 elliptocytosis 282.7 Hb-S (without crisis) 282.63 with crisis 282.64 vaso-occlusive pain 282.64 sickle-cell (without crisis) 282.63 with crisis 282.64 vaso-occlusive pain 282.64 thalassemia 282.49 constant spring 282.7 D (Hb-D) 282.7 with other abnormal hemoglobin NEC 282.7 Hb-S (without crisis) 282.68 with crisis 282.69 sickle-cell (without crisis) 282.68 with crisis 282.69 thalassemia 282.49 E (Hb-E) 282.7 with other abnormal hemoglobin NEC 282.7 Hb-S (without crisis) 282.68 with crisis 282.69 sickle-cell (without crisis) 282.68 with crisis 282.69 thalassemia 282.49 elliptocytosis 282.7 F (Hb-F) 282.7 G (Hb-G) 282.7 H (Hb-H) 282.49 hereditary persistence, fetal (HPFH) ("Swiss variety") 282.7 high fetal gene 282.7 I thalassemia 282.49 M 289.7 S - see also Disease, sickle-cell, Hb-S thalassemia (without crisis) 282.41 with crisis 282.42 vaso-occlusive pain 282.42 spherocytosis 282.7 unstable, hemolytic 282.7 Zurich (Hb-Zurich) 282.7 hemolytic (fetus) (newborn) 773.2 unstable hemoglobin 282.7 HPFH (hereditary persistence of fetal hemoglobin) ("Swiss variety") 282.7 unstable hemoglobin hemolytic 282.7 Elliptocytosis (congenital) (hereditary) 282.1 Hb-C (disease) 282.7 hemoglobin disease 282.7 Findings, abnormal, without diagnosis (examination) (laboratory test) 796.4 hematocrit elevated 282.7 hemoglobin elevated 282.7 Heinz-body anemia, congenital 282.7 Hemoglobin - see also condition fetal, hereditary persistence 282.7 Hemoglobinopathy (mixed) (see also Disease, hemoglobin) 282.7 with thalassemia 282.49 sickle-cell 282.60 with thalassemia (without crisis) 282.41 with crisis 282.42 vaso-occlusive pain 282.42 Persistence, persistent (congenital) 759.89 fetal hemoglobin (hereditary) ("Swiss variety") 282.7 hemoglobin, fetal (hereditary) (HPFH) 282.7 Spherocytosis (congenital) (familial) (hereditary) 282.0 hemoglobin disease 282.7 Trait hemoglobin abnormal NEC 282.7 with thalassemia 282.49 C (see also Disease, hemoglobin, C) 282.7 with elliptocytosis 282.7