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Brain small vessel disease with or without ocular anomalies
Disease Summary
Associated Targets (1)
Tbio
1
Uniprot Description An autosomal dominant disease characterized by weakening of the blood vessels in the brain and retinal arteriolar tortuosity. In affected individuals, stroke is often the first symptom and is usually caused by bleeding in the brain (hemorrhagic stroke) rather than a lack of blood flow in the brain (ischemic stroke). Patients also have leukoencephalopathy and may experience seizures and migraine headaches accompanied by visual sensations known as auras.
DataSource References
UniProt Disease: OMIM:607595
DisGeNET: UMLS:C4013035
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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 UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
UniProt Disease
DisGeNET
High level summary of knowledge for a disease, including descriptions and datasource references.