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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