Night Blindness, Congenital Stationary, Type 1f (CSNB1F)

Alias:

Congenital Stationary Night Blindness 1f

Csnb1f

Complete Congenital Stationary Night Blindness 1f Autosomal Recessive

Night Blindness, Congenital Stationary , 1f, Autosomal Recessive

Congenital Stationary Night Blindness 1f Autosomal Recessive

Blindness, Night, Stationary, Congenital, Type 1f

Night Blindness, Congenital Stationary, 1f

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 1f, also known as congenital stationary night blindness 1f, 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 1f is LRIT3 (Leucine Rich Repeat, Ig-Like And Transmembrane Domains 3). Related phenotypes are reduced visual acuity and nyctalopia

Related ID：

MALACARDS：NGH030

OMIM：615058

MESH：D009755