|
D56.1 |
Beta thalassemia |
| Billable Code | is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. |
| GEMS |
| ICD-10-CM D56.1 converts approximately to:ICD-9-CM |
| 2015 ICD-9-CM 282.44 Beta thalassemia |
| ICD-10-CM D56.1is grouped within Diagnostic Related Group(s) (MS-DRG v30.0) |
| 793 FULL TERM NEONATE WITH MAJOR PROBLEMS
|
| 811 RED BLOOD CELL DISORDERS WITH MCC
|
| 812 RED BLOOD CELL DISORDERS WITHOUT MCC
|
| Type 1 Excludes |
| beta thalassemia minor (D56.3) |
| beta thalassemia trait (D56.3) |
| delta-beta thalassemia (D56.2) |
| hemoglobin E-beta thalassemia (D56.5) |
| sickle-cell beta thalassemia (D57.4-) |
| Alternate Description |
| Beta thalassemia major |
| Cooley's anemia |
| Homozygous beta thalassemia |
| Severe beta thalassemia |
| Thalassemia intermedia |
| Thalassemia major |
| ICD-10-CM Index Entry |
| ICD-10-CM Index entries containing back-references to ICD-10-CM '.D56.1.' |
| Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); Cooley's (erythroblastic) |
| Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); erythroblastic; familial |
| Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); erythroblastic; of childhood |
| Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); familial erythroblastic |
| Cooley's anemia |
| Thalassemia (anemia) (disease); beta (severe) |
| Thalassemia (anemia) (disease); beta (severe); homozygous |
| Thalassemia (anemia) (disease); beta (severe); major |
| Thalassemia (anemia) (disease); intermedia |
| Thalassemia (anemia) (disease); major |
