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 282.49
Other thalassemia
- heterogeneous group of hereditary hemolytic anemias which have in common a decreased rate of synthesis of one or more hemoglobin polypeptide chains.
- Short description: Thalassemia NEC.
- ICD-9-CM 282.49 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 282.49.
- More recent version(s) of ICD-9-CM 282.49: 2012 2013.
282.49 Alternative Terminology
- ^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 constant spring trait
- Hemoglobin e/beta thalassemia disease
- Hemoglobin h disease
- Hemoglobin lepore trait
- Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster
- Hereditary persistence of fetal hemoglobin thalassemia
- Heterozygous thalassemia
- Homozygous alpha thalassemia
- Homozygous beta thalassemia
- 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 with other hemoglobinopathy
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
Convert 282.49 to ICD-10-CM 
ICD-9-CM 282.49 converts directly to:
- 2013 ICD-10-CM D56.8 Other thalassemias
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
- familial erythroblastic (microcytic) 282.49
- high A2 282.49
- leptocytosis (hereditary) 282.49
- Mediterranean (with hemoglobinopathy) 282.49
- microcytic (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
- 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
- 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
- Thalassemic variants 282.49
- Trait
- hemoglobin
- Lepore 282.49
with other abnormal hemoglobin NEC 282.49
- Variants, thalassemic 282.49
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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