DCHS1, dachsous cadherin-related 1, 8642

N. diseases: 100; N. variants: 8
Disease: Heterotopia, Periventricular, Autosomal Recessive ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842563
Disease: Heterotopia, Periventricular, Autosomal Recessive
Heterotopia, Periventricular, Autosomal Recessive 		0.300 Biomarker disease CTD_human Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development. 24056717 2013