STATH, statherin, 6779

N. diseases: 57; N. variants: 0
Disease: Autosomal dominant retinitis pigmentosa ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		0.010 Biomarker disease BEFREE Microsatellite (STR) markers tightly linked to genes known to be responsible for adRP were selected for linkage analysis. 23834559 2015