Night Blindness, Congenital Stationary, Type1i (CSNB1I)

Night Blindness, Congenital Stationary, Type1i(来自ICD-11)

别称:

Night Blindness, Congenital Stationary, Type 1i

Csnb1i

Night Blindness, Congenital Stationary, 1i

加入收藏

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Night Blindness, Congenital Stationary, Type1i, is also known as night blindness, congenital stationary, type 1i. An important gene associated with Night Blindness, Congenital Stationary, Type1i is GUCY2D (Guanylate Cyclase 2D, Retinal). Affiliated tissues include bone, and related phenotypes are nyctalopia and tritanomaly

查看原文参与反馈