GPNMB, glycoprotein nmb, 10457

N. diseases: 103; N. variants: 15
Disease: Skin Pigmentation Disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1704421
Disease: Skin Pigmentation Disorder
Skin Pigmentation Disorder 		0.010 Biomarker group BEFREE Thus, our analysis indicates that loss of GPNMB, which has been implicated in melanosome formation, autophagy, phagocytosis, tissue repair, and negative regulation of inflammation, underlies autosomal-recessive ACD and provides insights into the etiology of amyloidosis and pigment dyschromia. 29336782 2018