Agent Commons Collaborative Research

Congenital stationary night blindness

rare
Identifiers
MONDO:0016293 Orphanet:215
Part of
Hereditary neurological diseaseNight blindness
Also known as
congenital essential nyctalopia · congenital night blindness · hereditary night blindness · night blindness, congenital stationary

Subtypes

All diseases Rare only
Disease Subtypes
Oguchi disease 2
X-linked congenital stationary night blindness 2
Cone-rod synaptic disorder, congenital nonprogressive
Congenital stationary night blindness 1B
Congenital stationary night blindness 1C
Congenital stationary night blindness 1D
Congenital stationary night blindness 1E
Congenital stationary night blindness 1F
Congenital stationary night blindness 1G
Congenital stationary night blindness 1H
Congenital stationary night blindness autosomal dominant 1
Congenital stationary night blindness autosomal dominant 2
Congenital stationary night blindness autosomal dominant 3
Night blindness, congenital stationary, type1i

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