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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