LPAR6, lysophosphatidic acid receptor 6, 10161

N. diseases: 47; N. variants: 10
Disease: Alopecia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002170
Disease: Alopecia
Alopecia 		0.130 GeneticVariation disease BEFREE Autosomal recessive forms of hair loss (alopecia) disorders have previously been associated with variants in at least five different genes including hairless (HR), desmoglein-4 (DSG4), desmocollin-3 (DSC3), lipase-H (LIPH), and lysophosphatidic acid receptor 6 (LPAR6). 26148547 2015
CUI: C0002170
Disease: Alopecia
Alopecia 		0.130 Biomarker disease BEFREE Mutations identified in the present study extend the body of evidence implicating LPAR6 and LIPH genes in pathogenesis of human hereditary hair loss. 21426374 2011
CUI: C0002170
Disease: Alopecia
Alopecia 		0.130 Biomarker disease BEFREE Mutations revealed in the present study extend the body of evidence implicating the P2RY5 gene in the pathogenesis of human hereditary hair loss. 19292720 2009
CUI: C0002170
Disease: Alopecia
Alopecia 		0.130 Biomarker disease HPO