Gene: SPG11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.100 CausalMutation phenotype CLINVAR SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration. 19194956 2009
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.100 Biomarker phenotype HPO
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.100 GeneticVariation phenotype CLINVAR