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
|