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 disease BEFREE Homozygosity mapping and exome sequencing in two affected siblings of a consanguineous family with mild intellectual disability, spastic paraplegia, and strabismus revealed a homozygous premature stop mutation at codon 139 of C12ORF65. 24080142 2013
Entrez Id: 91574
Gene Symbol: C12orf65
C12orf65
0.110 Biomarker disease HPO