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 |
0 |
Phenotype entries for this disease |
0 |
Associated with 4 genes |
APOA2, EPHX2, GHR, LDLR |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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