Disease #00165 (ARH (hypercholesterolemia, familial, autosomal recessive (ARH)), OMIM:603813)

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	Curator: Johan T. den Dunnen

Official abbreviation	ARH
Name	hypercholesterolemia, familial, autosomal recessive (ARH)
OMIM ID	603813
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
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	N/A