Disease #00234 (FHCL3 (HYPERCHOLESTEROLEMIA, FAMILIAL, 3), OMIM:603776)

Official abbreviation FHCL3
Name HYPERCHOLESTEROLEMIA, FAMILIAL, 3
OMIM ID 603776
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PCSK9
Associated tissues -
Disease features -
Remarks -
Date created 2025-11-24 07:29:31 +00:00 (UTC)
Date last edited N/A

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