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reticular dystrophy of the retinal pigment epithelium
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Reticular dystrophy of the retinal pigment epithelium is a patterned dystrophy of the retinal pigment epithelium, of progressive course, characterized by the presence of a bilateral hyperpigmented reticular pattern resembling a fishnet with knots, resulting in a slowly progressive loss of vision that often only becomes apparent in old age. Reticular dystrophy of the retinal pigment epithelium is sometimes associated with scleral staphyloma, choroidal neovascularization, convergent strabismus, spherophakia with myopia and luxated lenses, and partial atrophy of the iris.
Mondo Term and Equivalent IDs
MONDO:0009979: reticular dystrophy of the retinal pigment epithelium
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
MESH:C564844
OMIM:267800
Orphanet:99002
MONDO:0009979
High level summary of knowledge for a disease, including descriptions and datasource references.