Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0746857
Disease: Focal Neurologic Deficits
Focal Neurologic Deficits
0.300 Biomarker phenotype CTD_human Maternofetal and neonatal copper requirements revealed by enterocyte-specific deletion of the Menkes disease protein. 23064757 2012
CUI: C0746857
Disease: Focal Neurologic Deficits
Focal Neurologic Deficits
0.300 Biomarker phenotype CTD_human Prenatal treatment of mosaic mice (Atp7a mo-ms) mouse model for Menkes disease, with copper combined by dimethyldithiocarbamate (DMDTC). 22815746 2012