Disease #00164 (FHCL3 (hypercholesterolemia, familial, type 3), OMIM:603776)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FHCL3
Name	hypercholesterolemia, familial, type 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	2013-07-01 16:08:07 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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