Disease #00148 (FHCL1 (HYPERCHOLESTEROLEMIA, FAMILIAL, 1), OMIM:143890)

Official abbreviation FHCL1
Name HYPERCHOLESTEROLEMIA, FAMILIAL, 1
OMIM ID 143890
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene LDLR
Associated tissues -
Disease features -
Remarks -

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