You are using an outdated browser. Please upgrade your browser to improve your experience.
Oguchi disease-1
Disease Summary
Associated Targets (2)
Tchem
1
Tbio
1
Mondo Description Any Oguchi disease in which the cause of the disease is a mutation in the SAG gene.
Uniprot Description A non-progressive retinal disorder characterized by impaired night vision, often associated with nystagmus and myopia. Congenital stationary night blindness Oguchi type is an autosomal recessive form associated with fundus discoloration and abnormally slow dark adaptation.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0110712
OMIM:258100
MONDO:0009775
High level summary of knowledge for a disease, including descriptions and datasource references.