Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy
0.010 GeneticVariation disease BEFREE Dysfunction of cGMP signalling in photoreceptors by a macular dystrophy-related mutation in the calcium sensor GCAP1. 28025326 2017