Night Blindness, Congenital Stationary, Type 1e (CSNB1E)

Alias:

Congenital Stationary Night Blindness 1e

Csnb1e

Night Blindness, Congenital Stationary , 1e, Autosomal Recessive

Congenital Stationary Night Blindness 1e Autosomal Recessive

Blindness, Night, Stationary, Congenital, Type 1e

Night Blindness, Congenital Stationary, Type 1

Night Blindness, Congenital Stationary, 1e

Csnb, Complete, Autosomal Recessive

Complete Autosomal Recessive Csnb

Csnb1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Night Blindness, Congenital Stationary, Type 1e, also known as congenital stationary night blindness 1e, 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 1e is GPR179 (G Protein-Coupled Receptor 179). Affiliated tissues include retina and eye, and related phenotypes are congenital stationary night blindness and nystagmus

Related ID：

MALACARDS：NGH029

OMIM：614565

MESH：D009755