RNF170, ring finger protein 170, 81790

N. diseases: 11; N. variants: 2
Disease: Spastic Paraplegia, Hereditary ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		0.010 GeneticVariation disease BEFREE Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia. 31636353 2019