SNURF, SNRPN upstream reading frame, 8926

N. diseases: 63; N. variants: 1
Disease: Amyotrophy, monomelic ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 15 2 0.010 None 1.000 1 2005 2005