Source: CLINVAR

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C1855465 STARGARDT DISEASE 1 (disorder) disease Disease or Syndrome genetic disease; disease of anatomical entity 6 210
C3495438 Macular Degeneration, Age-Related, 2 disease Eye Diseases Disease or Syndrome genetic disease; disease of anatomical entity 2 18
C1858806 CONE-ROD DYSTROPHY 3 (disorder) disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome genetic disease; disease of anatomical entity 1 41
C1866422 RETINITIS PIGMENTOSA 19 disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome genetic disease; disease of anatomical entity 1 22
C0271093 Stargardt's disease phenotype Disease or Syndrome genetic disease; disease of anatomical entity 1 12