SEMA4A, semaphorin 4A, 64218

N. diseases: 141; N. variants: 5
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 On variants and disease-causing mutations: Case studies of a SEMA4A variant identified in inherited blindness. 28805479 2018
CUI: C0456909
Disease: Blindness
Blindness 		0.110 Biomarker phenotype HPO