2009 ICD-9-CM Diagnosis Code 282.7 : Other hemoglobinopathies

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2009 ICD-9-CM Diagnosis Code 282.7

Other hemoglobinopathies

Short description: HEMOGLOBINOPATHIES NEC.
ICD-9-CM 282.7 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 282.7 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
You are viewing the 2009 version of ICD-9-CM 282.7.
More recent version(s) of ICD-9-CM 282.7: 2010 2011 2012 2013 2014 2015.

Convert to ICD-10-CM: 282.7 converts approximately to:

2015/16 ICD-10-CM D56.4 Hereditary persistence of fetal hemoglobin [HPFH]
Or:
2015/16 ICD-10-CM D58.2 Other hemoglobinopathies

Approximate Synonyms

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
Hemoglobinopathy, hereditary
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
Hgb C disease
Hgb C trait
Hgb D disease
Hgb D trait
Hgb E disease
Hgb E trait
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

familial polycythemia (289.6)
hemoglobin M [Hb-M] disease (289.7)
high-oxygen-affinity hemoglobin (289.0)

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

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
  - aplastic 284.01
  - due to isoimmunization NEC 773.2
  - Heinz-body 282.7
  - hereditary hemolytic NEC 282.9
  - nonspherocytic
    - type I 282.2
    - type II 282.3
  - pernicious 281.0
  - spherocytic (see also Spherocytosis) 282.0
- Heinz-body, congenital 282.7
- hemolytic 283.9
  - acquired 283.9
    - with hemoglobinuria NEC 283.2
    - autoimmune (cold type) (idiopathic) (primary) (secondary) (symptomatic) (warm type) 283.0
    - due to
      - cold reactive antibodies 283.0
      - drug exposure 283.0
      - warm reactive antibodies 283.0
    - fragmentation 283.19
    - idiopathic (chronic) 283.9
    - infectious 283.19
      - autoimmune 283.0
    - non-autoimmune 283.10
    - toxic 283.19
    - traumatic cardiac 283.19
  - acute 283.9
    - due to enzyme deficiency NEC 282.3
    - fetus or newborn (see also Disease, hemolytic) 773.2
      - late 773.5
    - Lederer's (acquired infectious hemolytic anemia) 283.19
  - 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
    - cardiac conditions 283.19
    - drugs 283.0
    - enzyme deficiency NEC 282.3
      - drug-induced 282.2
    - presence of shunt or other internal prosthetic device 283.19
    - thrombotic thrombocytopenic purpura 446.6
  - elliptocytotic (see also Elliptocytosis) 282.1
  - familial 282.9
  - hereditary 282.9
    - due to enzyme deficiency NEC 282.3
    - specified NEC 282.8
  - idiopathic (chronic) 283.9
  - infectious (acquired) 283.19
  - mechanical 283.19
  - microangiopathic 283.19
  - nonautoimmune 283.10
  - nonspherocytic
    - congenital or hereditary NEC 282.3
      - glucose-6-phosphate dehydrogenase deficiency 282.2
      - pyruvate kinase (PK) deficiency 282.3
      - type I 282.2
      - type II 282.3
    - type I 282.2
    - type II 282.3
  - 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
    - autoimmune 283.0
      - acute 285.1
  - 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
    - 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
  - autoimmune (cold type) (warm type) 283.0
  - due to or with
    - incompatibility
      - ABO (blood group) 773.1
      - blood (group) (Duffy) (Kell) (Kidd) (Lewis) (M) (S) NEC 773.2
      - Rh (blood group) (factor) 773.0
    - Rh negative mother 773.0
  - 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
  - drop (precipitous) 790.01
  - elevated 282.7
  - low 285.9
- hemoglobin
  - elevated 282.7
  - low 285.9
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
  - circulation 747.83
  - form of cervix (uteri) 752.49
  - hemoglobin (hereditary) ("Swiss variety") 282.7
  - pulmonary hypertension 747.83
- 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
  - S (Hb-S) 282.5

282.69

ICD9Data.com

282.8

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 2009 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.

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