Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 100359402
Gene Symbol: SPG41
SPG41
CUI: C3888208
Disease: SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT
SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT 		0.300 GermlineCausalMutation ORPHANET A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia. 18364116

2008