RPS6, ribosomal protein S6, 6194

N. diseases: 117; N. variants: 2
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: C0265252
Disease: Coffin-Lowry syndrome
Coffin-Lowry syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 23 25 0.030 None 1.000 3 2006 2016