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Browse Genes by Name

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  • oculocerebrorenal syndrome of Lowe: OCRL
  • oculocutaneous albinism II: OCA2
  • opsin 1 (cone pigments), long-wave-sensitive: OPN1LW
  • opsin 1 (cone pigments), medium-wave-sensitive: OPN1MW
  • opsin 1 (cone pigments), short-wave-sensitive: OPN1SW
  • optic atrophy 1 (autosomal dominant): OPA1
  • optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia): OPA3
  • oral-facial-digital syndrome 1: OFD1
  • origin recognition complex, subunit 1: ORC1
  • origin recognition complex, subunit 4: ORC4
  • origin recognition complex, subunit 6: ORC6
  • ornithine aminotransferase: OAT
  • ornithine carbamoyltransferase: OTC
  • orthodenticle homeobox 2: OTX2
  • otoferlin: OTOF
 
 
Published: July 27, 2015