| DISEASE NAME | NON RARE IN EUROPE: Heterozygous familial hypercholesterolemia |
| DISEASE CATEGORY (ICD10) | None524 |
| DISEASE ID (ICD10) | N.A. |
| DISEASE ID (OMIM) | N.A. |
| 9 combinations linked to 406 | OLI500; OLI817; OLI818; OLI819; OLI820; OLI821; OLI1215; OLI1304; OLI1305 |
| 4 gene combinations linked to 406 | CYP7A1; LRP6; LDLR; PCSK9; ABCG5; CD36; PCSK9; CYP7A1; LDLRAP1; LRP6 |
| ORPHANET ID | 406 |