Disease #00146 (FHCL2 (HYPERCHOLESTEROLEMIA, FAMILIAL, 2), OMIM:144010)

Official abbreviation FHCL2
Name HYPERCHOLESTEROLEMIA, FAMILIAL, 2
OMIM ID 144010
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene APOB
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-22 10:09:11 +00:00 (UTC)
Date last edited N/A

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