Night Blindness, Congenital Stationary, Type 2a (CSNB2A)

Alias:

Congenital Stationary Night Blindness 2a

Csnb2a

Csnb2

Night Blindness, Congenital Stationary, X-Linked, Type 2a

Night Blindness, Congenital Stationary , 2a, X-Linked

Congenital Stationary Night Blindness 2a X-Linked

Blindness, Night, Stationary, Congenital, Type 2a

Night Blindness, Congenital Stationary, Type 2

Congenital Stationary Night Blindness Type 2

Night Blindness, Congenital Stationary, 2a

Csnb, Incomplete, X-Linked

Incomplete X-Linked Csnb

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Night Blindness, Congenital Stationary, Type 2a, also known as congenital stationary night blindness 2a, is related to night blindness, congenital stationary, type 1a and x-linked congenital stationary night blindness. An important gene associated with Night Blindness, Congenital Stationary, Type 2a is CACNA1F (Calcium Voltage-Gated Channel Subunit Alpha1 F), and among its related pathways/superpathways is Visual signal transduction: Cones. Affiliated tissues include retina and eye, and related phenotypes are reduced visual acuity and electronegative electroretinogram

Related ID：

MALACARDS：NGH025

OMIM：300071

MESH：D009755