CLCN4, chloride voltage-gated channel 4, 1183

N. diseases: 114; N. variants: 14
Disease: MENTAL RETARDATION, X-LINKED 15 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0796221
Disease: MENTAL RETARDATION, X-LINKED 15
MENTAL RETARDATION, X-LINKED 15 		0.700 GeneticVariation disease UNIPROT X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes. 25644381 2016
CUI: C0796221
Disease: MENTAL RETARDATION, X-LINKED 15
MENTAL RETARDATION, X-LINKED 15 		0.700 Biomarker disease GENOMICS_ENGLAND X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes. 25644381 2016
CUI: C0796221
Disease: MENTAL RETARDATION, X-LINKED 15
MENTAL RETARDATION, X-LINKED 15 		0.700 Biomarker disease GENOMICS_ENGLAND Exome sequencing reveals new causal mutations in children with epileptic encephalopathies. 23647072 2013
CUI: C0796221
Disease: MENTAL RETARDATION, X-LINKED 15
MENTAL RETARDATION, X-LINKED 15 		0.700 GeneticVariation disease UNIPROT Exome sequencing reveals new causal mutations in children with epileptic encephalopathies. 23647072 2013
CUI: C0796221
Disease: MENTAL RETARDATION, X-LINKED 15
MENTAL RETARDATION, X-LINKED 15 		0.700 GeneticVariation disease CLINVAR
CUI: C0796221
Disease: MENTAL RETARDATION, X-LINKED 15
MENTAL RETARDATION, X-LINKED 15 		0.700 CausalMutation disease CLINVAR
CUI: C0796221
Disease: MENTAL RETARDATION, X-LINKED 15
MENTAL RETARDATION, X-LINKED 15 		0.700 Biomarker disease CTD_human