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Summary Literature (1)
MIM:258870 - GYRATE ATROPHY OF CHOROID AND RETINA; GACR

Xenbase Genes: oat.2, oat

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009796 - ornithine aminotransferase deficiency

Disease Ontology (DO):
DOID:1415 - gyrate atrophy