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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 3 (autosomal recessive, with chorea and spastic paraplegia):
OPA3
ornithine carbamoyltransferase:
OTC
otoferlin:
OTOF
Published: January 23, 2009
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