Congenital stationary night blindness 1G

MONDO:0014614

A congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the GNAT1 gene on chromosome 3p21.

Also known as: CSNB1G, congenital stationary night blindness type 1G, night blindness, congenital stationary, type 1G

34 clinical trials for this condition and its sub-types, 0 tagged with Congenital stationary night blindness 1G itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal recessive disease (999) ↑ Congenital nervous system disorder (287) ↑ Congenital stationary night blindness (5)

Including sub-types (34) Tagged with Congenital stationary night blindness 1G (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.