Night Blindness, Congenital Stationary, Type 1c (CSNB1C)

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

别称:

Congenital Stationary Night Blindness 1c

Csnb1c

Night Blindness, Congenital Stationary , 1c, Autosomal Recessive

Congenital Stationary Night Blindness 1c Autosomal Recessive

Blindness, Night, Stationary, Congenital, Type 1c

Night Blindness, Congenital Stationary, Type Ic

Night Blindness, Congenital Stationary, 1c

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 1c, also known as congenital stationary night blindness 1c, is related to night blindness, congenital stationary, type 1e and night blindness, congenital stationary, type 1b. An important gene associated with Night Blindness, Congenital Stationary, Type 1c is TRPM1 (Transient Receptor Potential Cation Channel Subfamily M Member 1). Affiliated tissues include skin, and related phenotypes are reduced visual acuity and congenital stationary night blindness

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