ICD 10 CM Codes

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