Disease #00031 (FH (Familial hypercholesterolemia))
| Official abbreviation |
FH |
| Name |
Familial hypercholesterolemia |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
23 |
| Phenotype entries for this disease |
14 |
| Associated with 5 genes |
ABCG8, APOB, LDLR, LDLRAP1, PCSK9 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-11-29 09:15:44 +08:00 (CST) |
| Date last edited |
N/A |
Individuals
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