GPC1, glypican 1, 2817

N. diseases: 96; N. variants: 3
Disease: Albright's hereditary osteodystrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931404
Disease: Albright's hereditary osteodystrophy
Albright's hereditary osteodystrophy 		0.010 Biomarker disease BEFREE GPC1 and/or STK25 haploinsufficiency may also contribute to the AHO-like phenotype. 15521982 2004