CABP4, calcium binding protein 4, 57010

N. diseases: 29; N. variants: 11
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.
Amaurosis congenita of Leber, type 1
disease Eye Diseases Disease or Syndrome 81 60 0.010 None 1.000 1 2010 2010
Night blindness, congenital stationary
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 32 52 0.620 strong 1.000 2 2006 2010
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
disease Eye Diseases Disease or Syndrome 168 18 0.120 None 1.000 2 2006 2012
Incomplete congenital stationary night blindness
disease Disease or Syndrome 3 2 0.020 None 1.000 2 2004 2009