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OAT
: ornithine aminotransferase
OCA2
: oculocutaneous albinism II
OCRL
: oculocerebrorenal syndrome of Lowe
OFD1
: oral-facial-digital syndrome 1
OPA1
: optic atrophy 1 (autosomal dominant)
OPA3
: optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
OPN1LW
: opsin 1 (cone pigments), long-wave-sensitive
OPN1MW
: opsin 1 (cone pigments), medium-wave-sensitive
OPN1SW
: opsin 1 (cone pigments), short-wave-sensitive
OTC
: ornithine carbamoyltransferase
OTOF
: otoferlin
OTX2
: orthodenticle homeobox 2
OXCT1
: 3-oxoacid CoA transferase 1
Published: February 11, 2013