CCNO, cyclin O, 10309

N. diseases: 67; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.120 GeneticVariation disease BEFREE Our results further establish <i>CCNO</i> as an important gene for normal development and suggest that heterozygous CCNO mutations could underlie hydrocephalus or diminished fertility in some human patients. 29245899 2017
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.120 Biomarker disease BEFREE Combining these 15 patients with the previously reported CCNO case reports revealed rapid deterioration in lung function, an increased prevalence of hydrocephalus (10%) as well as increased female infertility (22%). 26777464 2016
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.120 Biomarker disease HPO