retinitis pigmentosa type 36 (RP36)

Genetics

• associated with defects in PRCD gene

Clinical manifestations

• presents as difficulty seeing at night as a child

More general terms

• retinitis pigmentosa (RP)

Additional terms

• progressive rod-cone degeneration protein (PRCD)

Database

• OMIM: https://mirror.omim.org/entry/608380