Disease #01380 (FCHL3 (hyperlipidemia, combined, familial), OMIM:144250)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	FCHL3
Name	hyperlipidemia, combined, familial
OMIM ID	144250
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LPL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2023-05-02 16:34:24 +02:00 (CEST)

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