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GTR Home > Conditions/Phenotypes > Choroidal dystrophy, central areolar, 1

Choroidal dystrophy, central areolar, 1

Summary

Any central areolar choroidal dystrophy in which the cause of the disease is a mutation in the GUCY2D gene. [from MONDO]

Available tests

11 tests are in the database for this condition.

Clinical tests (11 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CACD, CACD1, CG-E, CORD5, CORD6, CSNB1I, CYGD, GUC1A4, GUC2D, LCA, LCA1, RCD2, RETGC-1, ROS-GC1, ROSGC, retGC, GUCY2D
    Summary: guanylate cyclase 2D, retinal

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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