Disease #00148 (FHCL1 (HYPERCHOLESTEROLEMIA, FAMILIAL, 1), OMIM:143890)

MVZ für Humangenetik Regensburg

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Official abbreviation	FHCL1
Name	HYPERCHOLESTEROLEMIA, FAMILIAL, 1
OMIM ID	143890
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LDLR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-27 08:44:04 +00:00 (UTC)
Date last edited	2023-06-27 08:45:53 +00:00 (UTC)