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ENCone-Rod Dystrophy 20 (CORD20)
Alias:
Cord20
Dystrophy, Cone-Rod, Type 20
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Cone-Rod Dystrophy 20, also known as cord20, is related to retinitis pigmentosa 1 and cone-rod dystrophy 18. An important gene associated with Cone-Rod Dystrophy 20 is POC1B (POC1 Centriolar Protein B), and among its related pathways/superpathways is Ciliopathies. Affiliated tissues include retina and bone, and related phenotypes are nystagmus and reduced visual acuity
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