night blindness, congenital stationary, type1i
MONDO:0032811Mondo
Findings
No curated finding names night blindness, congenital stationary, type1i yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
2 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.
- NyctalopiaHPOHP:0000662
- 5 of 5 reported patients · Childhood onset
- TritanomalyHPOHP:0000552
- 2 of 5 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- GUCY2DHGNC:4689
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
Where it sits
Other names
2 names
Resolves to: night blindness, congenital stationary, type1i
- Also called
- CSNB1Inight blindness, congenital stationary, type 1I