CUL4B, cullin 4B, 8450

N. diseases: 162; N. variants: 17
Disease: Congenital Abnormality ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.010 GeneticVariation group BEFREE This interaction might contribute to the development of cerebral malformations in patients with variants in CUL4B. 25385192 2015