Disease: Forebrain Defects ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1861235
Disease: Forebrain Defects
Forebrain Defects 		0.110 GeneticVariation disease BEFREE A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects. 12073012 2002
CUI: C1861235
Disease: Forebrain Defects
Forebrain Defects 		0.110 CausalMutation disease CLINVAR