KIF1B, kinesin family member 1B, 23095

N. diseases: 213; N. variants: 16
Disease: Spastic Paraplegia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		0.010 Biomarker disease BEFREE This gene is involved in typical CMT2A and in more atypical phenotypes as optic atrophy or spastic paraplegia. 26686600 2016