retinitis pigmentosa type 37 (RP37)

Genetics

• autosomal dominant
• associated with defects in NR2E3 gene

More general terms

• retinitis pigmentosa (RP)

Additional terms

• photoreceptor-specific nuclear receptor (retina-specific nuclear receptor, nuclear receptor subfamily 2 group E member 3, NR2E3, PNR, RNR)

Database

• OMIM: https://mirror.omim.org/entry/611131