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DOID:1415 - gyrate atrophy
Disease Ontology Definition:n_a
Synonyms: Gyrate atrophy of the choroid and/or retina, Ornithinemia with gyrate atrophy, gyrate atrophy of the retina,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0009796 - ornithine aminotransferase deficiency |
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)