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Norum disease
Summary
- Synonym
-
- LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
- lecithin acyltransferase deficiency
- Super Class
- hypolipoproteinemia
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1946 | EFNA5 | ephrin A5 | |
| 2822 | GPLD1 | glycosylphosphatidylinositol specific phospholipase D1 | |
| 3030 | HADHA | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | |
| 3032 | HADHB | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | |
| 3290 | HSD11B1 | hydroxysteroid 11-beta dehydrogenase 1 | |
| 3339 | HSPG2 | heparan sulfate proteoglycan 2 | |
| 3931 | LCAT | lecithin-cholesterol acyltransferase | |
| 3956 | LGALS1 | galectin 1 | |
| 4023 | LPL | lipoprotein lipase | |
| 5286 | PIK3C2A | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001084 | Corneal arcus |
| HP:0003233 | Decreased HDL cholesterol concentration |
| HP:0000083 | Renal insufficiency |
| HP:0003651 | Foam cells |
| HP:0001895 | Normochromic anemia |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0002155 | Hypertriglyceridemia |
| HP:0000093 | Proteinuria |
| HP:0003581 | Adult onset |
| HP:0001878 | Hemolytic anemia |
