KLHL7, kelch like family member 7, 55975

N. diseases: 135; N. variants: 14
Disease: Retinal Diseases ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		0.110 GeneticVariation group BEFREE Mutation screening of KLHL7 in 502 retinopathy probands has revealed three different missense mutations in six independent families. 19520207 2009
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		0.110 Biomarker group HPO