PDE6H, phosphodiesterase 6H, 5149

N. diseases: 33; N. variants: 1
Disease: Dyschromatopsia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia 		0.110 GeneticVariation disease BEFREE Recently, the human PDE6H gene was identified as a novel locus for autosomal recessive (incomplete) color blindness. 25739440 2015
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia 		0.110 Biomarker disease HPO