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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 7

Retinitis pigmentosa 7

Synonyms
RP 7

Summary

A retinitis pigmentosa that has material basis in mutation in the PRPH2 gene on chromosome 6p21. [from MONDO]

Available tests

60 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (60 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: AOFMD, AVMD, CACD2, DS, MDBS1, PRPH, RDS, RP7, TSPAN22, rd2, PRPH2
    Summary: peripherin 2

  • Also known as: ROM, ROSP1, RP7, TSPAN23, ROM1
    Summary: retinal outer segment membrane protein 1

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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