Iga Vasculitis
Disease ID: disease_node_6461
Connections displayed (default: 10).
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| Dbxref | GARD:8204, ICD10CM:D69.0, ICD9CM:287.0, MESH:D011695, NCI:C34963, SNOMEDCT_US_2023_03_01:191306005, UMLS_CUI:C0034152 |
|---|---|
| Subclassof | DOID_9809 |
| Data Source | DOID, MESH |
| Synonyms | Allergic purpura, Autoimmune purpura, Henoch-Sch?nlein purpura, Henoch-Sch@nlein purpura, Henoch-Scholein purpura, Henoch-Schonlein Purpura, Purpura, autoimmune |
| Mesh Id | D011695 |
| Mesh Label | IgA Vasculitis |
| Mesh Subclassof | D007105, D011693, D017445, D020141, D014657 |
| Doid Label | Henoch-Schoenlein purpura |
| Doid 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. |
| Disease Node Id | disease_node_6461 |
| Doid Id | DOID_11123 |
| Label | Iga Vasculitis |
- Outgoing r'ship
SUBCLASS_OFto/from Vasculitis, Leukocytoclastic, Cutaneous(ID:disease_node_9685) (Disease)