Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013949
Disease: Embryopathies
Embryopathies
0.300 Biomarker disease CTD_human Mutant CHUK and severe fetal encasement malformation. 20961246 2010
CUI: C0013949
Disease: Embryopathies
Embryopathies
0.300 Biomarker disease CTD_human Limb and skin abnormalities in mice lacking IKKalpha. 10195895 1999
CUI: C0013949
Disease: Embryopathies
Embryopathies
0.300 Biomarker disease CTD_human Abnormal morphogenesis but intact IKK activation in mice lacking the IKKalpha subunit of IkappaB kinase. 10195896 1999
CUI: C0013949
Disease: Embryopathies
Embryopathies
0.300 Biomarker disease CTD_human IKK1-deficient mice exhibit abnormal development of skin and skeleton. 10346820 1999