Night Blindness, Congenital Stationary, Type 1d (CSNB1D)

Night Blindness, Congenital Stationary, Type 1d(来自ICD-11)

别称:

Congenital Stationary Night Blindness 1d

Csnb1d

Night Blindness, Congenital Stationary , 1d, Autosomal Recessive

Congenital Stationary Night Blindness 1d Autosomal Recessive

Blindness, Night, Stationary, Congenital, Type 1d

Night Blindness, Congenital Stationary, 1d

Csnb, Complete, Autosomal Recessive

Complete Autosomal Recessive Csnb

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Night Blindness, Congenital Stationary, Type 1d, also known as congenital stationary night blindness 1d, is related to night blindness, congenital stationary, type 1b and night blindness, congenital stationary, type 1c. An important gene associated with Night Blindness, Congenital Stationary, Type 1d is SLC24A1 (Solute Carrier Family 24 Member 1), and among its related pathways/superpathways is Visual Cycle in Retinal Rods. Related phenotypes are congenital stationary night blindness and pigmentary retinopathy

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