U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 97

Retinitis pigmentosa 97

Summary

Retinitis pigmentosa-97 (RP97) is characterized by onset of night blindness and visual field defects in the first decade of life, with later onset of reduced visual acuity (Kong et al., 2023). For a general phenotypic description and a discussion of genetic heterogeneity of RP, see 268000. [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: KIAA0564, P7BP2, RP97, VWA8
    Summary: von Willebrand factor A domain containing 8

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.