Home > 2011 ICD-9-CM Diagnosis Codes > Diseases Of The Blood And Blood-Forming Organs 280-289 > Hereditary hemolytic anemias 282-
2011 ICD-9-CM Diagnosis Code 282.7
Other hemoglobinopathies
- group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
- Short description: Hemoglobinopathies NEC.
- ICD-9-CM 282.7 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
- You are viewing the 2011 version of ICD-9-CM 282.7.
- More recent version(s) of ICD-9-CM 282.7: 2012 2013.
282.7 Alternative Terminology
- Acquired heinz body anemia
- Acquired hemoglobinopathy
- Arthropathy secondary to hemoglobinopathy
- Decreased erythrocyte life span
- Double heterozygous sickling disorder
- Heinz bodies
- Hematopoietic maturation arrest
- Hemoglobin a1c above reference range
- Hemoglobin c disease
- Hemoglobin c trait
- Hemoglobin d disease
- Hemoglobin d trait
- Hemoglobin e disease
- Hemoglobin e trait
- Hemoglobin low
- Hemoglobin o-arab trait
- Hemoglobin very high
- Hemoglobin zurich disease
- Hemoglobinopathy
- Hemoglobinopathy with cyanosis
- Hemoglobinopathy with erythrocytosis
- Hereditary hemoglobinopathy
- Hereditary hemoglobinopathy due to globin chain mutation
- Hereditary persistence of fetal hemoglobin
- Hereditary persistence of fetal hemoglobin a gamma beta^+^ thalassemia
- Hereditary persistence of fetal hemoglobin deletion type
- Hereditary persistence of fetal hemoglobin delta beta^0^ thalassemia
- Hereditary persistence of fetal hemoglobin g gamma beta^+^ thalassemia
- Hereditary persistence of fetal hemoglobin nondeletion type
- Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster
- Heterozygous hemoglobinopathy
- High affinity hemoglobin
- Homozygous hemoglobinopathy
- Increased erythrocyte destruction
- Increased heme-heme interaction
- Low affinity hemoglobin
- Mixed hemoglobin disorder
- Osteonecrosis due to hemoglobinopathy
- Red blood cell destruction finding
- Sickle cell retinopathy
- Thalassemia-hemoglobin c disease
- Unstable hemoglobin disease
282.7 Excludes 
Applies To
- 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
Convert 282.7 to ICD-10-CM
ICD-9-CM Volume 2 Index entries containing back-references to 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, congenital 282.7
- hemolytic 283.9
- acquired 283.9
- acute 283.9
- autoimmune (acquired) 283.0
- chronic 282.9
idiopathic 283.9
- cold type (secondary) (symptomatic) 283.0
- congenital (spherocytic) (see also Spherocytosis) 282.0
- nonspherocytic - see Anemia, hemolytic, nonspherocytic, congenital
- drug-induced 283.0
- enzyme deficiency 282.2
- due to
- elliptocytotic (see also Elliptocytosis) 282.1
- familial 282.9
- hereditary 282.9
- idiopathic (chronic) 283.9
- infectious (acquired) 283.19
- mechanical 283.19
- microangiopathic 283.19
- nonautoimmune 283.10
- nonspherocytic
- of or complicating pregnancy 648.2
- resulting from presence of shunt or other internal prosthetic device 283.19
- secondary 283.19
- autoimmune 283.0
- sickle-cell - see Disease, sickle-cell
- Stransky-Regala type (Hb-E) (see also Disease, hemoglobin) 282.7
- symptomatic 283.19
- toxic (acquired) 283.19
- uremic (adult) (child) 283.11
- warm type (secondary) (symptomatic) 283.0
- 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
- constant spring 282.7
- D (Hb-D) 282.7
- E (Hb-E) 282.7
- 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
- spherocytosis 282.7
- unstable, hemolytic 282.7
- Zurich (Hb-Zurich) 282.7
- hemolytic (fetus) (newborn) 773.2
- 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
- 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
- Persistence, persistent (congenital) 759.89
- fetal
- hemoglobin, fetal (hereditary) (HPFH) 282.7
- Spherocytosis (congenital) (familial) (hereditary) 282.0
- hemoglobin disease 282.7
- Trait
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 282.7 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2011 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
|
Free 2013 ICD-9-CM Codes
|
Free 2013 ICD-10-CM/PCS Codes
|
|
Free 2007-2012 ICD-9-CM Codes
|
Free 2007-2013 HCPCS Codes
|
|
Site Information
|