Disease: Blindness ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0456909
Disease: Blindness
Blindness 		0.110 GeneticVariation phenotype BEFREE We describe a novel mutation in the previously identified MFSD8 gene in a family with a common phenotype of LINCL, but no clinical report of vision loss. 18850119 2009
CUI: C0456909
Disease: Blindness
Blindness 		0.110 Biomarker phenotype HPO