Disease #05708 (FHCL1 (hypercholesterolemia, familial, type 1 (FHCL1)), OMIM:143890)
| Official abbreviation |
FHCL1 |
| Name |
hypercholesterolemia, familial, type 1 (FHCL1) |
| OMIM ID |
143890 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 4 genes |
APOA2, EPHX2, GHR, LDLR |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-02-26 12:52:07 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|