U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 32

Retinitis pigmentosa 32

Synonyms
RP 32

Summary

A retinitis pigmentosa that has material basis in variation in the chromosome region 1p21.3-p13.3. [from MONDO]

Available tests

2 tests are in the database for this condition.

Clinical tests (2 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: MCLC, RP32, CLCC1
    Summary: chloride channel CLIC like 1

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

Show allHide all

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.