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D70.0 |
Congenital agranulocytosis |
| Billable Code | is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. |
| GEMS |
| ICD-10-CM D70.0 converts approximately to:ICD-9-CM |
| 2015 ICD-9-CM 288.01 Congenital neutropenia |
| ICD-10-CM D70.0is grouped within Diagnostic Related Group(s) (MS-DRG v30.0) |
| 808 MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH MCC
|
| 809 MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH CC
|
| 810 MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITHOUT CC/MCC
|
| Alternate Description |
| Congenital neutropenia |
| Infantile genetic agranulocytosis |
| Kostmann's disease |
| ICD-10-CM Index Entry |
| ICD-10-CM Index entries containing back-references to ICD-10-CM '.D70.0.' |
| Agranulocytosis (chronic) (cyclical) (genetic) (infantile) (periodic) (pernicious); congenital |
| Aleukia; congenital |
| Disease, diseased; Kostmann's (infantile genetic agranulocytosis) |
| Leukopenia; congenital |
| Leukopenia; cyclic |
| Leukopenia; familial |
| Leukopenia; infantile genetic |
| Leukopenia; periodic |
| Neutropenia, neutropenic (chronic) (genetic) (idiopathic) (immune) (infantile) (malignant) (pernicious) (splenic); congenital (primary) |
| Syndrome; Kostmann's |
