eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hypercholesterolemia, familial |
| Symptom | C0010068|coronary artery disease |
| Sentences | 5 |
| PubMedID- 24175066 | Objective: to assess the relationship of levels of inflammatory risk markers to presence of clinical coronary artery disease (cad) in patients with treated heterozygous familial hypercholesterolaemia. |
| PubMedID- 22434290 | Suboptimal consideration and management of potential familial hypercholesterolaemia in patients with suspected premature coronary artery disease. |
| PubMedID- 23411100 | Carotid plaque burden as a measure of subclinical coronary artery disease in patients with heterozygous familial hypercholesterolemia. |
| PubMedID- 22419126 | Abca1 gene promoter dna methylation is associated with hdl particle profile and coronary artery disease in familial hypercholesterolemia. |
| PubMedID- 23519510 | familial hypercholesterolaemia presenting with coronary artery disease in a young patient. |
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