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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 69

Retinitis pigmentosa 69

Summary

Retinitis pigmentosa (RP), also designated rod-cone dystrophy, is characterized by initial night blindness due to rod dysfunction, with subsequent progressive constriction of visual fields, abnormal color vision, and eventual loss of central vision due to cone photoreceptor involvement (summary by El Shamieh et al., 2014). For a discussion of genetic heterogeneity of retinitis pigmentosa, see 268000. [from OMIM]

Available tests

10 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (10 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: C20orf19, HT013, Kizuna, NCRNA00153, PLK1S1, RP69, KIZ
    Summary: kizuna centrosomal protein

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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