PDYN, prodynorphin, 5173

N. diseases: 197; N. variants: 13
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4310780
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23 		0.010 Biomarker disease BEFREE Spinocerebellar Ataxia 23 (SCAR23) is a newly described condition caused by mutations in TDP2 gene. 31410782 2019