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exudative vitreoretinopathy 4

http://purl.obolibrary.org/obo/DOID_0111411

An exudative vitreoretinopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in LRP5 on chromosome 11q13.2. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

exudative vitreoretinopathy 4

Synonyms

EVR4

database cross reference

has obo namespace

disease_ontology

DOID:0111411

Term relations

Subclass of:

exudative vitreoretinopathy
autosomal genetic disease
has material basis in some autosomal inheritance