SNURF, SNRPN upstream reading frame, 8926

N. diseases: 63; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic
0.010 GeneticVariation disease BEFREE To report the results of a comprehensive evaluation of clinical, magnetic resonance imaging (MRI), electromyography (EMG), and survival motor neuron (SMN) gene analysis of HD. 15642858 2005