Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23327
Gene Symbol: NEDD4L
NEDD4L
CUI: C0265553
Disease: Polysyndactyly
Polysyndactyly 		0.300 Biomarker CTD_human Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia. 27694961

2016