Disease #00165 (FHCL4 (hypercholesterolemia, familial, type 4), OMIM:603813)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FHCL4
Name	hypercholesterolemia, familial, type 4
OMIM ID	603813
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LDLRAP1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-07-01 16:16:04 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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