2013 ICD-9-CM Diagnosis Code 282.0 : Hereditary spherocytosis

includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.
autosomal dominant trait marked by splenomegaly, jaundice, and fragile, spheroid erythrocytes which are prematurely cleared by the spleen; anemia is usually mild; treatment is splenectomy.
ICD-9-CM 282.0 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.

282.0 Excludes

Applies To

Convert 282.0 to ICD-10-CM

ICD-9-CM Volume 2 Index entries containing back-references to 282.0:

Acholuric jaundice (familial) (splenomegalic) (see also Spherocytosis) 282.0
- acquired 283.9
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
- 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
- spherocytic (hereditary) (see also Spherocytosis) 282.0
Disease, diseased - see also Syndrome
- Holla (see also Spherocytosis) 282.0
Holla disease (see also Spherocytosis) 282.0
Icteroanemia, hemolytic (acquired) 283.9
- congenital (see also Spherocytosis) 282.0
Icterus (see also Jaundice) 782.4
- hemolytic (acquired) 283.9
  - congenital (see also Spherocytosis) 282.0
Jaundice (yellow) 782.4
- acholuric (familial) (splenomegalic) (see also Spherocytosis) 282.0
  - acquired 283.9
- hemolytic (acquired) 283.9
  - congenital (see also Spherocytosis) 282.0
Minkowski-Chauffard syndrome (see also Spherocytosis) 282.0
Spherocytosis (congenital) (familial) (hereditary) 282.0
- hemoglobin disease 282.7
- sickle-cell (disease) 282.60
Syndrome - see also Disease
- Minkowski-Chauffard (see also Spherocytosis) 282.0

282

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282.1

ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 282.0 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 2013 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.

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