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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 35

Retinitis pigmentosa 35

Synonyms
RP 35

Summary

Retinitis pigmentosa-35 (RP35) is characterized by night blindness with progressive loss of vision. Pigment deposits and narrowing of vasculature are seen in the retina (Abid et al., 2006). Mutation in SEMA4A can also cause a form of cone-rod dystrophy (CORD10; 610283). For a general phenotypic description and a discussion of genetic heterogeneity of retinitis pigmentosa, see 268000. [from OMIM]

Available tests

27 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (27 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CORD10, RP35, SEMAB, SEMB, SEMA4A
    Summary: semaphorin 4A

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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