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Bradyopsia
1 OMIM reference -
2 associated genes
5 connected diseases
2 signs/symptoms
Disease Type of connection
Early infantile epileptic encephalopathy
Congenital stationary night blindness
Central areolar choroidal dystrophy
Cone rod dystrophy
Leber congenital amaurosis
Synonym(s):
- PERRS
- Prolonged electroretinal response supression

Classification (Orphanet):
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the eye and adnexa -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: no data available
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
RGS9 O75916604067
RGS9BP Q6ZS82607814
Very frequent
- Mild visual loss / impaired visual acuity
- Photophobia