congenital stationary night blindness
MONDO:0016293Mondo
Findings
No curated finding names congenital stationary night blindness yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
14 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal dark-adapted electroretinogramHPOHP:0030469
- Very frequent (80% to 99% of cases)
- MyopiaHPOHP:0000545
- Very frequent (80% to 99% of cases)
- NyctalopiaHPOHP:0000662
- Very frequent (80% to 99% of cases)
- Reduced visual acuityHPOHP:0007663
- Very frequent (80% to 99% of cases)
- Early-onset non-progressive night blindnessHPOHP:0007642
- Frequent (30% to 79% of cases)
- NystagmusHPOHP:0000639
- Frequent (30% to 79% of cases)
- StrabismusHPOHP:0000486
- Frequent (30% to 79% of cases)
- Compensatory head postureHPOHP:0031705
- Occasional (5% to 29% of cases)
- ERG: Reduced dark-adapted b-wave amplitudeHPOHP:0007984
- Occasional (5% to 29% of cases)
- HypermetropiaHPOHP:0000540
- Occasional (5% to 29% of cases)
- Reduced amplitude of dark-adapted bright flash electroretinogram a-waveHPOHP:0030483
- Occasional (5% to 29% of cases)
- Abnormal retinal pigmentationHPOHP:0007703
- Very rare (1% to 4% of cases)
Show the remaining 2
- Color vision defectHPOHP:0000551
- Very rare (1% to 4% of cases)
- Retinal thinning on OCTHPOHP:0030329
- Very rare (1% to 4% of cases)
Where it sits
- Narrower terms (14)
- 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
- Oguchi disease
- X-linked congenital stationary night blindness
Other names
4 names
Resolves to: congenital stationary night blindness
- Also called
- congenital essential nyctalopiacongenital night blindnesshereditary night blindnessnight blindness, congenital stationary