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Oguchi disease-2

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any Oguchi disease in which the cause of the disease is a mutation in the GRK1 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 associated with fundus discoloration and abnormally slow dark adaptation.
Mondo Term and Equivalent IDs
MONDO:0013259:  Oguchi disease-2
UMLS:C3150678: