Disease: Optic Atrophy 1 ×
Source: BEFREE ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0338508
Disease: Optic Atrophy 1
Optic Atrophy 1 		0.020 GeneticVariation disease BEFREE To evaluate a family with autosomal dominant optic atrophy, which has been previously linked to the Kidd blood group. 10369594 1999
CUI: C0338508
Disease: Optic Atrophy 1
Optic Atrophy 1 		0.020 GeneticVariation disease BEFREE A second locus for dominant optic atrophy has recently been shown to map to chromosome 18q12.2-12.3 near the Kidd blood group locus. 9783700 1998