OAT, ornithine aminotransferase, 4942

N. diseases: 92; N. variants: 71
Disease: Gyrate Atrophy ×
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: C0018425
Disease: Gyrate Atrophy
Gyrate Atrophy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 8 35 1.000 definitive 0.962 52 35 1981 2019