Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55280
Gene Symbol: CWF19L1
CWF19L1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.010 GeneticVariation BEFREE A zebrafish model showed that CWF19L1 loss-of-function mutations result in abnormal cerebellar morphology and movement disorders. 27016154

2016