Disease #00174 (FH (hypercholesterolemia, familial (FH)), OMIM:143890)

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	Curator: Johan T. den Dunnen

Official abbreviation	FH
Name	hypercholesterolemia, familial (FH)
OMIM ID	143890
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 7 genes	ABCA1, APOA2, EPHX2, GHR, ITIH4, LDLR, PPP1R17
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-08-11 14:06:36 +02:00 (CEST)
Date last edited	N/A