gyrate atrophy

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Summary

Literature (0)

DOID:1415 - gyrate atrophy

Disease Ontology Definition:n_a

Synonyms: Gyrate atrophy of the choroid and/or retina, gyrate atrophy of the retina, Ornithinemia with gyrate atrophy

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: oat.2, oat

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009796 - ornithine aminotransferase deficiency

MONDO:0009796 - ornithine aminotransferase deficiency

MIM:

MIM:258870 - GYRATE ATROPHY OF CHOROID AND RETINA; GACR

MIM:258870 - GYRATE ATROPHY OF CHOROID AND RETINA; GACR

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): choroid disease (is_a)