Gene: FTL ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2512
Gene Symbol: FTL
FTL 		0.110 GeneticVariation phenotype BEFREE Mutations in the ferritin light chain cause an adult-onset autosomal-dominant choreiform movement disorder termed neuroferritinopathy. 21496576 2011
Entrez Id: 2512
Gene Symbol: FTL
FTL 		0.110 Biomarker phenotype HPO