2012 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 2012 version of ICD-9-CM 282.49.
- More recent version(s) of ICD-9-CM 282.49: 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
282.49 Excludes
Applies To
- Dominant thalassemia
- Hemoglobin C thalassemia
- Hereditary leptocytosis
- Mediterranean anemia (with other hemoglobinopathy)
- Mixed thalassemia
- Thalassemia with other hemoglobinopathy
Mediterranean 282.40
with hemoglobinopathy 282.49
