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Henoch-Schoenlein purpura
Disease Summary
Associated Targets (2)
Tclin
1
Tchem
1
Mondo Description A systemic, usually self-limited immune complex vasculitis, characterized by immunoglobulin A deposition in the small vessels and kidneys. It is manifested with small hemorrhages in the skin, gastrointestinal symptoms, arthritis, and nephropathy.
Disease Ontology Description A hypersensitivity vasculitis that is characterized by purpura (purplish plaques), arthralgia, gastrointestinal upset, and/or glomerulonephritis, and may be related to increased immune response following an infection.
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 Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:11123
EFO:1000965
ICD9:287.0
MESH:D011695
NCIT:C34963
SCTID:191306005
MONDO:0006785
High level summary of knowledge for a disease, including descriptions and datasource references.