Gene: CLCN4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1183
Gene Symbol: CLCN4
CLCN4 		0.100 CausalMutation phenotype CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844 2018