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DO Term : bradyopsia 1 [DOID:0070363] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A braydopsia that has_material_basis_in homozygous or compound heterozygous mutation in the RGS9 gene on chromosome 17q24.

synonyms:
608415,
prolonged electroretinal response suppression 1,
OMIM:608415

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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