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Browse Genes by Symbol

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OCA2: oculocutaneous albinism II
OCRL: oculocerebrorenal syndrome of Lowe
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

Published: January 23, 2009