Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4047
Gene Symbol: LSS
LSS
CUI: C0002170
Disease: Alopecia
Alopecia 		0.420 GeneticVariation BEFREE We expanded the phenotypic spectrum of LSS to a recessive neuroectodermal syndrome formerly named alopecia with mental retardation (APMR) syndrome. 30723320

2019
Entrez Id: 4047
Gene Symbol: LSS
LSS
CUI: C0002170
Disease: Alopecia
Alopecia 		0.420 Biomarker BEFREE The identification of LSS as causal gene for autosomal-recessive HS highlights the importance of the cholesterol pathway in hair follicle biology and may facilitate novel therapeutic approaches for hair loss disorders in general. 30401459

2018