|
E78.71 |
Barth syndrome |
| Billable Code | is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. |
| GEMS |
| ICD-10-CM E78.71 converts approximately to:ICD-9-CM |
| 2015 ICD-9-CM 759.89 Other specified congenital anomalies |
| ICD-10-CM E78.71is grouped within Diagnostic Related Group(s) (MS-DRG v30.0) |
| 564 OTHER MUSCULOSKELETAL SYSTEM AND CONNECTIVE TISSUE DIAGNOSES WITH MCC
|
| 565 OTHER MUSCULOSKELETAL SYSTEM AND CONNECTIVE TISSUE DIAGNOSES WITH CC
|
| 566 OTHER MUSCULOSKELETAL SYSTEM AND CONNECTIVE TISSUE DIAGNOSES WITHOUT CC/MCC
|
| Alternate Description |
| Abetalipoproteinemia |
| Depressed HDL cholesterol |
| High-density lipoprotein deficiency |
| Hypoalphalipoproteinemia |
| Hypobetalipoproteinemia (familial) |
| Lecithin cholesterol acyltransferase deficiency |
| Tangier disease |
| ICD-10-CM Index Entry |
| ICD-10-CM Index entries containing back-references to ICD-10-CM '.E78.71.' |
| Barth syndrome |
| Disorder (of); bile acid and cholesterol metabolism; Barth syndrome |
| Disorder (of); cholesterol and bile acid metabolism; Barth syndrome |
| Syndrome; Barth |
