2012 ICD-9-CM Diagnosis Code 282.1 : Hereditary elliptocytosis

intrinsic defect of erythrocytes inherited as an autosomal dominant trait; erythrocytes assume an oval or elliptical shape.
Short description: Heredit elliptocytosis.
ICD-9-CM 282.1 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
You are viewing the 2012 version of ICD-9-CM 282.1.
More recent version(s) of ICD-9-CM 282.1: 2013.

Applies To

Convert 282.1 to ICD-10-CM

ICD-9-CM Volume 2 Index entries containing back-references to 282.1:

Anemia 285.9
- elliptocytosis (see also Elliptocytosis) 282.1
- 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
- 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

282.0

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282.2

ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 282.1 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 2012 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.

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