Disease: Spastic paraplegia 4, autosomal dominant ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		0.010 GeneticVariation disease BEFREE The partial heterozygous deletion of DPY30 could modify the phenotypic expression of SPG4 patients with this pedigree. 20857310 2011