SNURF, SNRPN upstream reading frame, 8926

N. diseases: 63; N. variants: 1
Disease: Myelopathic Muscular Atrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0270765
Disease: Myelopathic Muscular Atrophy
Myelopathic Muscular Atrophy 		0.010 GeneticVariation disease BEFREE Deletions in the SMN gene in infantile and adult spinal muscular atrophy patients from the same family. 8786072 1996