Rare diseases · Sign or symptom
Early-onset non-progressive night blindness
Night blindness since birth
HP:0007642
What it means
A usually nonprogressive (i.e., stationary) form of night blindness with early (presumed to be congenital) onset.
Congenital stationary night blindness is the result of either dysfunction of the rod photoreceptors or synaptic transmission. This term was previously called Congenital stationary night blindness. The terms hemeralopia and nyctalopia are deliberately not used, as they mean different things in different languages. The fundus can be either normal or abnormal, such as fundus with white dots in fundus albipunctatus, or a golden sheen in light-adapted state in Oguchi disease, which disappears with dark-adaptation (Mizuo-Nakamura phenomenon).
Rare diseases that can present with this12
Very common80–99%
8- 15q overgrowth syndrome
- Chondroectodermal dysplasia with night blindness
- Duplication of the pituitary gland
- FGFR2-related bent bone dysplasia
- Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome
- Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome
- Oguchi disease
- X small rings syndrome
Common30–79%
3The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Congenital night blindness · Congenital stationary night blindness · Night blindness, congenital · Night blindness, congenital stationary · Night blindness, congenital stationary, complete · Night blindness, stationary
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Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.