Opportunities for Engaging Long-Term and Post-Acute Care Providers in Health Information Exchange Activities: Exchanging Interoperable Patient Assessment Information. Hyperlipidemia

12/01/2011

(Excel file available at: http://aspe.hhs.gov/daltcp/reports/2011/SE-D/Hyperlipidemia.xls)

Refset Name: Hyperlipidemia refset
  refset_ID   SCTID FSN
831 13644009 Hypercholesterolemia (disorder)
831   55822004 Hyperlipidemia (disorder)
831 3.98E+08 Fredrickson type IIa hyperlipoproteinemia (disorder)
831 3.98E+08 Familial hypercholesterolemia (disorder)
831 33513003 Familial apolipoprotein C-II deficiency (disorder)
831 2.67E+08 Familial hyperchylomicronemia (disorder)
831 2.38E+08 Fredrickson type I hyperlipoproteinemia (disorder)
831 34349009 Familial type 5 hyperlipoproteinemia (disorder)
831 34528009 Familial hypertriglyceridemia (disorder)
831 2.38E+08 Primary hypertriglyceridemia (disorder)
831 2.67E+08 Mixed hyperlipidemia (disorder)
831 2.99E+08 Familial multiple lipoprotein-type hyperlipidemia (disorder)
831 2.38E+08 Familial combined hyperlipidemia (disorder)
831 57218003 Cholesterol ester storage disease (disorder)
831 2.38E+08 Primary hypercholesterolemia (disorder)
831 1.3E+08 Endogenous hyperlipidemia (disorder)
831 1.3E+08 Exogenous hyperlipidemia (disorder)
831 1.3E+08 Mixed hypercholesterolemia and hypertriglyceridemia (disorder)
831 2.67E+08 Pure hypercholesterolemia (disorder)
831 2.67E+08 Pure hyperglyceridemia (disorder)
831 1.91E+08 Hyperlipidemia, group A (disorder)
831 2.38E+08 Very low density lipoprotinemia (disorder)
831 2.38E+08 Fredrickson type IV hyperlipoproteinemia (disorder)
831 2.38E+08 Primary combined hyperlipidemia (disorder)
831 2.38E+08 Polygenic hypercholesterolemia (disorder)
831 2.38E+08 Familial hypercholesterolemia - homozygous (disorder)
831 2.38E+08 Familial hypercholesterolemia - heterozygous (disorder)
831 2.38E+08 Hyperalphalipoproteinemia (disorder)
831 2.38E+08 Familial defective apolipoprotein B-100 (disorder)
831 2.38E+08 Secondary hypercholesterolemia (disorder)
831 3.03E+08 Hypertriglyceridemia (disorder)
831 2.38E+08 Secondary hypertriglyceridemia (disorder)
831 2.38E+08 Secondary combined hyperlipidemia (disorder)
831 4.02E+08 Sporadic primary hypertriglyceridemia (disorder)
831 4.02E+08 Primary "polygenic" type Iib combined hyperlipidemia (disorder)
831 4.02E+08 Primary acquired chylomicronemia (disorder)
831 4.03E+08 Primary chylomicronemia (disorder)
831 4.03E+08 Hyperlipidemia with lipid deposition in skin (disorder)
831 4.03E+08 Secondary hyperlipidemia (disorder)
831 4.03E+08 Primary genetic hyperlipidemia (disorder)
831 4.03E+08 Chylomicronemia syndrome (disorder)
831 4.03E+08 Primary genetic mixed hyperlipidemia (disorder)
831 4.04E+08 Familial lipoprotein lipase deficiency with type I phenotype (disorder)
831 4.04E+08 Familial lipoprotein lipase deficiency with type V phenotype (disorder)
831 4.04E+08 Familial hypercholesterolemia due to heterozygous LDL receptor mutation (disorder)
831 4.04E+08 Familial hypercholesterolemia due to homozygous LDL receptor mutation (disorder)
831 4.04E+08 Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
831 4.26E+08 Chemically induced hyperlipidemia (disorder)
831 4.45E+08 Posttransplant hyperlipidemia (disorder)

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