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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 88

Retinitis pigmentosa 88

Summary

Retinitis pigmentosa-88 (RP88) is characterized by night blindness and constriction of peripheral visual fields, with mildly reduced visual acuity. Examination shows typical findings of RP, including attenuated retinal vessels, pale optic discs, and pigment deposits in the peripheral retinal pigment epithelium (Zobor et al., 2018; Hu et al., 2019; Albarry et al., 2019). For a discussion of genetic heterogeneity of RP, see 268000. [from OMIM]

Available tests

4 tests are in the database for this condition.

Clinical tests (4 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: DCDC4B, OCMD, RP88, RP1L1
    Summary: RP1 like 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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