Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye
0.100 GeneticVariation phenotype CLINVAR De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability. 29100089 2017
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye
0.100 CausalMutation phenotype CLINVAR De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability. 29100089 2017