Alphabetic Index · main term
Bürger-Grütz disease or syndrome
Bürger-Grütz disease or syndrome is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists E78.3 for this term: Hyperchylomicronemia. It is a billable code. Confirm any code you find here in the Tabular List before you report it.
Code the Index gives
Hyperchylomicronemia
Other Index terms that lead to E78.3
Different words, same code. 17 entries
- Chylomicronemia (fasting) (with hyperprebetalipoproteinemia)
- Disease, diseased, Bürger-Grütz (essential familial hyperlipemia)
- Disease, diseased, chylomicron retention
- Frederickson's hyperlipoproteinemia, type, I and V
- Hepatosplenomegaly, hyperlipemic (Bürger-Grütz type)
- 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
Show 5 more
- 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