Details of Disease

General Information of Disease (ID: DIST8K6C)

Disease Name Bradyopsia
Synonyms bradyopsia; PERRS; prolonged electroretinal response suppression
Definition Bradyopsia is characterized by prolonged electroretinal response suppression leading to difficulties adjusting to changes in luminance, normal to subnormal acuity and photophobia.
Disease Hierarchy
DISB4B0F: Retinopathy
DISD715V: Hereditary neurological disease
DIST8K6C: Bradyopsia
Disease Identifiers
MONDO ID
MONDO_0012033
MESH ID
C564243
UMLS CUI
C1842073
MedGen ID
331206
HPO ID
HP:0030511
Orphanet ID
75374
SNOMED CT ID
711163009

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
RGS9 OTRA1LOC Definitive Autosomal recessive [1]
RGS9BP OTE0U1OQ Definitive Autosomal recessive [1]
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References

1 Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation. Nature. 2004 Jan 1;427(6969):75-8. doi: 10.1038/nature02170.