CCNQ, cyclin Q, 92002

N. diseases: 56; N. variants: 4
Disease: Hypomagnesemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151723
Disease: Hypomagnesemia
Hypomagnesemia 		0.010 GeneticVariation phenotype BEFREE The dysfunction of CNNM family proteins is responsible for inherited hypomagnesemia, as well as various intractable diseases, such as cancer and hypertension. 30476181 2019