Disease: Nyctalopia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		0.110 Biomarker disease BEFREE These findings suggest that ffERG and cCSNB genetic testing should be considered for children who present with early-onset myopia, especially in the presence of strabismus and/or nystagmus, and that TRPM1-associated cCSNB is a channelopathy that may present without complaints of night blindness in childhood. 29522070 2018
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		0.110 Biomarker disease HPO