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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 61

Retinitis pigmentosa 61

Summary

Retinitis pigmentosa-61 (RP61) is an autosomal recessive photoreceptor degenerative disorder initially characterized by impairment of night vision and midperipheral visual field loss. Bone spicule pigmentation in the retinal periphery is present, and loss of rod function is detected by electroretinography (ERG) (Khan et al., 2011). For a general phenotypic description and a discussion of genetic heterogeneity of retinitis pigmentosa (RP), see 268000. [from OMIM]

Available tests

50 tests are in the database for this condition.

Clinical tests (50 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: RP61, USH3, USH3A, CLRN1
    Summary: clarin 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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