bradyopsia 2

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Summary

Literature (0)

DOID:0070364 - bradyopsia 2

Disease Ontology Definition:A braydopsia that has_material_basis_in homozygous mutation in the RGS9BP gene on chromosome 19q13.

Synonyms: prolonged electroretinal response suppression 2

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): bradyopsia (is_a)