retinitis pigmentosa type 10 (RP10)

Genetics

• autosomal dominant
• associated with defects in IMPDH1 gene

More general terms

• retinitis pigmentosa (RP)

Additional terms

• inosine-5'-monophosphate dehydrogenase 1; IMP dehydrogenase 1; IMPD 1; IMPDH 1; IMPDH-I (IMPDH1, IMPD1)

Database

• OMIM: https://mirror.omim.org/entry/180105