Gene: C12orf65 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 91574
Gene Symbol: C12orf65
C12orf65 		0.110 GeneticVariation phenotype BEFREE Considering our findings, we now conclude that truncating mutations in C12ORF65 lead to a variable phenotype with intellectual disability, spastic paraplegia, and ophthalmoplegia as common symptoms. 24080142 2013
Entrez Id: 91574
Gene Symbol: C12orf65
C12orf65 		0.110 Biomarker phenotype HPO