Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225210
Disease: OOCYTE MATURATION DEFECT 2
OOCYTE MATURATION DEFECT 2
0.600 GeneticVariation disease UNIPROT Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos. 27273344 2016
CUI: C4225210
Disease: OOCYTE MATURATION DEFECT 2
OOCYTE MATURATION DEFECT 2
0.600 GeneticVariation disease UNIPROT Mutations in TUBB8 and Human Oocyte Meiotic Arrest. 26789871 2016
CUI: C4225210
Disease: OOCYTE MATURATION DEFECT 2
OOCYTE MATURATION DEFECT 2
0.600 CausalMutation disease CLINVAR
CUI: C4225210
Disease: OOCYTE MATURATION DEFECT 2
OOCYTE MATURATION DEFECT 2
0.600 Biomarker disease CTD_human