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DO Term : exudative vitreoretinopathy 4 [DOID:0111411] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An exudative vitreoretinopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the LRP5 gene on chromosome 11q13.2.

synonyms:
MESH:C566619,
EVR4,
601813,
OMIM:601813

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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