Disease #05930 (STSL2 (sitosterolemia, type 2 (STSL2)), OMIM:618666)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curator: Global Variome, with Curator vacancy

Official abbreviation	STSL2
Name	sitosterolemia, type 2 (STSL2)
OMIM ID	618666
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ABCG5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-05-07 17:47:32 +02:00 (CEST)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.