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DO Term : bradyopsia 2 [DOID:0070364] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A braydopsia that has_material_basis_in homozygous mutation in the RGS9BP gene on chromosome 19q13.

synonyms:
OMIM:620344,
prolonged electroretinal response suppression 2,
620344

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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