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ENNight Blindness, Congenital Stationary, Type 1c (CSNB1C)
Alias:
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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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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