Night Blindness, Congenital Stationary, Type 1g (CSNB1G)

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

别称:

Congenital Stationary Night Blindness 1g

Csnb1g

Blindness, Night, Stationary, Congenital, Type 1g

Congenital Stationary Night Blindness Type 1g

Night Blindness, Congenital Stationary, 1g

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Night Blindness, Congenital Stationary, Type 1g, is also known as congenital stationary night blindness 1g. An important gene associated with Night Blindness, Congenital Stationary, Type 1g is GNAT1 (G Protein Subunit Alpha Transducin 1). Affiliated tissues include bone, and related phenotypes are rod-cone dystrophy and optic disc pallor

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