DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Disease: Lissencephaly and agenesis of corpus callosum ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1848070
Disease: Lissencephaly and agenesis of corpus callosum
Lissencephaly and agenesis of corpus callosum 		0.120 GeneticVariation disease BEFREE Our results indicate that in the Japanese, as has been seen elsewhere, abnormality of the DCX gene is the common cause of SCLH and ILS. 10807542 2000
CUI: C1848070
Disease: Lissencephaly and agenesis of corpus callosum
Lissencephaly and agenesis of corpus callosum 		0.120 Biomarker disease BEFREE These results provide strong evidence that loss of function of doublecortin is the major cause of SCLH. 9618162 1998
CUI: C1848070
Disease: Lissencephaly and agenesis of corpus callosum
Lissencephaly and agenesis of corpus callosum 		0.120 CausalMutation disease CLINVAR