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optic atrophy
Disease Summary
Associated Targets (31)
Tbio
16
Tclin
11
Tchem
4
Mondo Description A disorder characterized by loss of optic nerve fibers. It may be inherited or acquired. Acquired causes include ischemia, optic nerve neuropathy, glaucoma, trauma, radiation, brain tumors, and multiple sclerosis. It leads to vision disturbances.
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.
COHD:372914
DOID:5723
ICD10:H47.2
ICD9:377.10
MESH:D009896
NCIT:C34863
SCTID:76976005
UMLS:C0029124
UMLS:C1744705
MONDO:0003608
High level summary of knowledge for a disease, including descriptions and datasource references.