DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Disease: Double cortex ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931857
Disease: Double cortex
Double cortex 		0.040 Biomarker disease BEFREE Spontaneous epileptic manifestations in a DCX knockdown model of human double cortex. 20164125 2010
CUI: C2931857
Disease: Double cortex
Double cortex 		0.040 GeneticVariation disease BEFREE The microdeletion contains the X-linked Alport syndrome gene COL4A5, the MR genes FACL4 and PAK3, and parts of the X-chromosomal lissencephaly gene DCX associated with double cortex formation in girls, MR, and epilepsy. 19444485 2009
CUI: C2931857
Disease: Double cortex
Double cortex 		0.040 Biomarker disease BEFREE Classical lissencephaly and double cortex (subcortical band heterotopia): LIS1 and doublecortin. 10987567 2000
CUI: C2931857
Disease: Double cortex
Double cortex 		0.040 GeneticVariation disease BEFREE We and others have identified a novel brain specific gene, doublecortin, that is mutated in Double Cortex/X-linked lissencephaly (DC/XLIS) patients. 10515162 1999