partial central choroid dystrophy

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Summary

Literature (0)

DOID:9822 - partial central choroid dystrophy

Disease Ontology Definition:n_a

Synonyms: Choroidal dystrophy, central areolar

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

: prph2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0004890 - partial central choroid dystrophy

MONDO:0004890 - partial central choroid dystrophy

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

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

Parent(s): hereditary choroidal atrophy (is_a)