|
E78.3 |
Hyperchylomicronemia |
| Billable Code | is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. |
| GEMS |
| ICD-10-CM E78.3 converts approximately to:ICD-9-CM |
| 2015 ICD-9-CM 272.3 Hyperchylomicronemia |
| ICD-10-CM E78.3is grouped within Diagnostic Related Group(s) (MS-DRG v30.0) |
| 642 INBORN AND OTHER DISORDERS OF METABOLISM
|
| Alternate Description |
| Chylomicron retention disease |
| Fredrickson's hyperlipoproteinemia, type I or V |
| Hyperlipidemia, group D |
| Mixed hyperglyceridemia |
| ICD-10-CM Index Entry |
| ICD-10-CM Index entries containing back-references to ICD-10-CM '.E78.3.' |
| Bürger-Grütz disease or syndrome |
| Chylomicronemia (fasting) (with hyperprebetalipoproteinemia) |
| Disease, diseased; Bürger-Grütz (essential familial hyperlipemia) |
| Disease, diseased; chylomicron retention |
| Frederickson's hyperlipoproteinemia, type; I and V |
| Hyperchylomicronemia (familial) (primary) |
| Hyperchylomicronemia (familial) (primary); with hyperbetalipoproteinemia |
| Hyperglyceridemia (endogenous) (essential) (familial) (hereditary) (pure); mixed |
| Hyperlipemia, hyperlipidemia; group; D |
| Hyperlipoproteinemia; Fredrickson's type; I |
| Hyperlipoproteinemia; Fredrickson's type; V |
| Lipemia; retina, retinalis |
| Lipidosis; hepatosplenomegalic |
| Prebetalipoproteinemia (acquired) (essential) (familial) (hereditary) (primary) (secondary); with chylomicronemia |
| Syndrome; Bürger-Grütz |
| Xanthoma (s), xanthomatosis (primary) (familial) (hereditary); with; hyperlipoproteinemia; Type I |
| Xanthoma (s), xanthomatosis (primary) (familial) (hereditary); with; hyperlipoproteinemia; Type V |
