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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 56

Retinitis pigmentosa 56

Summary

Retinitis pigmentosa-56 (RP56) is an early-onset form of RP with progressive visual-field loss and deterioration of visual acuity (Bandah-Rozenfeld et al., 2010). For a general phenotypic description and a discussion of genetic heterogeneity of retinitis pigmentosa, see 268000. [from OMIM]

Available tests

30 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (30 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: IPM200, RP56, SPACRCAN, VMD5, IMPG2
    Summary: interphotoreceptor matrix proteoglycan 2

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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