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congenital stationary night blindness

MONDO:0016293

Also known as: Oguchi's disease, congenital essential nyctalopia, congenital night blindness, hereditary night blindness, night blindness, congenital stationary

MONDO:
MONDO:0016293
Orphanet:
215
Rare disease88 associated genes

Associated genes

+78 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.