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GTR Home > Conditions/Phenotypes > Retinal cone dystrophy 4

Retinal cone dystrophy 4

Summary

Any cone dystrophy in which the cause of the disease is a mutation in the CACNA2D4 gene. [from MONDO]

Available tests

24 tests are in the database for this condition.

Clinical tests (24 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: RCD4, CACNA2D4
    Summary: calcium voltage-gated channel auxiliary subunit alpha2delta 4

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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