NDN, necdin, MAGE family member, 4692

N. diseases: 124; N. variants: 2
Disease: Global developmental delay ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.120 Biomarker disease BEFREE We found that loss of Necdin decreased the number of functional LICs and enhanced myeloid differentiation <i>in vivo</i>, leading to delayed development of leukemia induced by MLL-AF9. 29152105 2017
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.120 Biomarker disease BEFREE NDN is one of several genes inactivated in Prader-Willi syndrome (PWS), a developmental disorder characterized by obesity, hypotonia, and developmental delay. 20665884 2010
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.120 Biomarker disease HPO