Congenital stationary night blindness 2A

MONDO:0010241

Any congenital stationary night blindness in which the cause of the disease is a mutation in the CACNA1F gene.

Also known as: CACNA1F congenital stationary night blindness, CSNB, incomplete, X-linked, congenital stationary night blindness caused by mutation in CACNA1F, congenital stationary night blindness type 2A, night blindness, congenital stationary (incomplete), 2A, X-linked, CSNB2A, night blindness, congenital stationary, type 2, night blindness, congenital stationary, type 2A

46 clinical trials for this condition and its sub-types, 0 tagged with Congenital stationary night blindness 2A itself.

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Including sub-types (46) Tagged with Congenital stationary night blindness 2A (0)

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