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age related macular degeneration 8
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any age-related macular degeneration in which the cause of the disease is a mutation in the ARMS2 gene.
Uniprot Description A form of age-related macular degeneration, a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane.
Disease Ontology Description An age related macular degeneration that has material basis in mutation in the ARMS2 gene, originally designated LOC387715, on chromosome 10q26.
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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.
Description from UniProt.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0110020
OMIM:613778
UMLS:C3151070
MONDO:0013416
High level summary of knowledge for a disease, including descriptions and datasource references.