Home > 2012 ICD-9-CM Diagnosis Codes > Diseases Of The Blood And Blood-Forming Organs 280-289 > Hereditary hemolytic anemias 282-
2012 ICD-9-CM Diagnosis Code 282.43
Alpha thalassemia
- ICD-9-CM 282.43 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 282.43.
- More recent version(s) of ICD-9-CM 282.43: 2013.
282.43 Excludes 
Applies To
- Alpha thalassemia major
- Hemoglobin H Constant Spring
- Hemoglobin H disease
- Hydrops fetalis due to alpha thalassemia
- Severe alpha thalassemia
- Triple gene defect alpha thalassemia
Convert 282.43 to ICD-10-CM
ICD-9-CM 282.43 converts directly to:
- 2013 ICD-10-CM D56.0 Alpha thalassemia
ICD-9-CM Volume 2 Index entries containing back-references to 282.43:
- Alpha thalassemia 282.43
- Disease, diseased - see also Syndrome
hemoglobin (Hb) 282.7
with thalassemia 282.49- abnormal (mixed) NEC 282.7
with thalassemia 282.49
- AS genotype 282.5
- Bart's 282.43
- 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) 282.43
- 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
- Hemoglobin - see also condition
- H Constant Spring 282.43
- H disease 282.43
- Hydrops 782.3
- Thalassemia (disease) 282.40
- alpha (major) (severe) (triple gene defect) 282.43
- silent carrier 282.46
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 282.43 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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