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Summary Literature (0)
MIM:613105 - CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2; CACD2

Xenbase Genes: prph2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0004890 - partial central choroid dystrophy
MONDO:0008982 - fascia
MONDO:0013137 - choroidal dystrophy, central areolar 2

Disease Ontology (DO):
DOID:9822 - partial central choroid dystrophy