CCND2, cyclin D2, 894

N. diseases: 241; N. variants: 15
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1845668
Disease: Perisylvian syndrome
Perisylvian syndrome
0.300 Biomarker disease CTD_human A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus. 29642246 2018