Search Ontology:
Human Disease

bradyopsia 1

Term ID
DOID:0070363
Synonyms
  • prolonged electroretinal response suppression 1
Definition
A braydopsia that has_material_basis_in homozygous or compound heterozygous mutation in the RGS9 gene on chromosome 17q24. (2)
References
Ontology
Human Disease   ( DOID:0070363 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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