2011 ICD-9-CM Diagnosis Code 282.49 : Other thalassemia

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2011 ICD-9-CM Diagnosis Code 282.49

Other thalassemia

Short description: Thalassemia NEC.
ICD-9-CM 282.49 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 282.49 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 2011 version of ICD-9-CM 282.49.
More recent version(s) of ICD-9-CM 282.49: 2012 2013 2014 2015.

Convert to ICD-10-CM: 282.49 converts directly to:

2015/16 ICD-10-CM D56.8 Other thalassemias

Approximate Synonyms

^A^gamma delta beta^0^ thalassemia
A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis
Acquired hemoglobin H disease
alpha Thalassemia
Alpha thalassemia-2 trait
Alpha thalassemia-mental retardation syndrome
Alpha trait thalassemia
alpha^+^ Thalassemia
alpha^+^ Thalassemia, deletion type
alpha^+^ Thalassemia, nondeletion type
alpha^0^ Thalassemia
Alpha-beta thalassemia
beta Thalassemia
Beta thalassemia intermedia
Beta thalassemia trait
beta^+^ Thalassemia
beta^+^ Thalassemia, normal Hb A>2<, type 1, silent
beta^+^ Thalassemia, normal Hb A>2<, type 2
beta^0^ Thalassemia
beta^0^ Thalassemia, deletion type
beta^0^ Thalassemia, nondeletion type
delta beta Thalassemia
delta beta^0^ Thalassemia
delta Thalassemia
delta^0^ Thalassemia
Delta-beta-Lepore thalassemia
epsilon gamma delta beta Thalassemia
epsilon gamma delta beta^0^ Thalassemia
Gamma thalassemia
Hb Lepore thalassemia
Hemoglobin Bart's hydrops syndrome
Hemoglobin C/beta thalassemia disease
Hemoglobin Constant Spring trait
Hemoglobin D/beta thalassemia disease
Hemoglobin E/beta thalassemia disease
Hemoglobin H constant spring thalassemia
Hemoglobin H disease
Hemoglobin Lepore trait
Hereditary persistence of fetal hemoglobin
Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster
Hereditary persistence of fetal hemoglobin thalassemia
Heterozygous thalassemia
Hgb C beta thalassemia
Hgb constant spring trait
Hgb D beta thalassemia
Hgb H constant spring disease
Homozygous alpha thalassemia
Homozygous beta thalassemia
Homozygous hemoglobin H constant spring thalassemia
Homozygous Hgb constant spring
Leptocytosis
Leptospirosis icterohemorrhagica
Sickle cell anemia with coexistent alpha-thalassemia
Sickle cell trait with coexistent alpha-thalassemia
Sickle cell-beta^+^-thalassemia
Sickle cell-beta^0^-thalassemia
Sickle cell-beta-thalassemia
Sickle cell-delta beta^0^-thalassemia
Sickle cell-thalassemia disease
Thalassemia
Thalassemia intermedia
Thalassemia major
Thalassemia syndrome
Thalassemia trait
Thalassemia trait, alpha
Thalassemia trait, beta
Thalassemia with other hemoglobinopathy
Thalassemia, alpha
Thalassemia, hemoglobin C beta
Thalassemia, hemoglobin constant spring carrier
Thalassemia, hemoglobin D beta
Thalassemia, hemoglobin H constant spring disease
Thalassemia, homozygous hemoglobin constant spring
Thalassemia, persistence of fetal hemoglobin

Applies To

Cooley's anemia
Hb-Bart's disease
Hereditary leptocytosis
Mediterranean anemia (with other hemoglobinopathy)
Microdrepanocytosis
Thalassemia (alpha) (beta) (intermedia) (major) (minima) (minor) (mixed) (trait) (with other hemoglobinopathy)
Thalassemia NOS

ICD-9-CM Volume 2 Index entries containing back-references to 282.49:

Alpha thalassemia 282.49
Anemia 285.9
- Cooley's (erythroblastic) 282.49
- erythroblastic
  - familial 282.49
  - fetus or newborn (see also Disease, hemolytic) 773.2
    - late 773.5
- familial erythroblastic (microcytic) 282.49
- high A2 282.49
- leptocytosis (hereditary) 282.49
- Mediterranean (with hemoglobinopathy) 282.49
- microcytic (hypochromic) 280.9
  - due to blood loss (chronic) 280.0
    - acute 285.1
  - familial 282.49
  - hypochromic 280.9
- microdrepanocytosis 282.49
- Rietti-Greppi-Micheli (thalassemia minor) 282.49
- target cell (oval) 282.49
- thalassemia 282.49
Beta thalassemia (major) (minor) (mixed) 282.49
Cooley's anemia (erythroblastic) 282.49
Dameshek's syndrome (erythroblastic anemia) 282.49
Disease, diseased - see also Syndrome
- Cooley's (erythroblastic anemia) 282.49
- 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
- high fetal gene or hemoglobin thalassemia 282.49
- Mediterranean (with hemoglobinopathy) 282.49
- microdrepanocytic 282.49
Hemoglobinopathy (mixed) (see also Disease, hemoglobin) 282.7
- with thalassemia 282.49
High
- A2 anemia 282.49
Lepore hemoglobin syndrome 282.49
Leptocytosis, hereditary 282.49
Mediterranean
- anemia (with other hemoglobinopathy) 282.49
- disease or syndrome (hemipathic) 282.49
Micheli-Rietti syndrome (thalassemia minor) 282.49
Microdrepanocytosis (thalassemia-Hb-S disease) 282.49
Rietti-Greppi-Micheli anemia or syndrome 282.49
Silvestroni-Bianco syndrome (thalassemia minima) 282.49
Syndrome - see also Disease
- Dameshek's (erythroblastic anemia) 282.49
- Lepore hemoglobin 282.49
- Micheli-Rietti (thalassemia minor) 282.49
- Rietti-Greppi-Micheli (thalassemia minor) 282.49
- Silvestroni-Bianco (thalassemia minima) 282.49
Target-oval cell anemia 282.49
Thalassanemia 282.49
Thalassemia (alpha) (beta) (disease) (Hb-C) (Hb-D) (Hb-E) (Hb-H) (Hb-I) (high fetal gene) (high fetal hemoglobin) (intermedia) (major) (minima) (minor) (mixed) (trait) (with other hemoglobinopathy) 282.49
- Hb-S (without crisis) 282.41
  - with
    - crisis 282.42
    - vaso-occlusive pain 282.42
- sickle-cell (without crisis) 282.41
  - with
    - crisis 282.42
    - vaso-occlusive pain 282.42
Thalassemic variants 282.49
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
- Lepore 282.49
  - with other abnormal hemoglobin NEC 282.49
Variants, thalassemic 282.49

282.42

ICD9Data.com

282.5

ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 282.49 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.

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