Postinfectious vasculitis
diseaseOn this page
Summary
Postinfectious vasculitis (MONDO:0018837) is a disease. A subtype of secondary vasculitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Prevalence: Unknown (Worldwide)
- Phenotypes (HPO): 57
Clinical features
Signs & symptoms
Clinical features (HPO)
57 HPO clinical features (Orphanet curated; top 50 by frequency):
| HPO ID | Term | Frequency |
|---|---|---|
| HP:0000099 | Glomerulonephritis | Frequent (30-79%) |
| HP:0001824 | Weight loss | Frequent (30-79%) |
| HP:0001945 | Fever | Frequent (30-79%) |
| HP:0002039 | Anorexia | Frequent (30-79%) |
| HP:0002829 | Arthralgia | Frequent (30-79%) |
| HP:0003326 | Myalgia | Frequent (30-79%) |
| HP:0005368 | Abnormality of humoral immunity | Frequent (30-79%) |
| HP:0010876 | Abnormal circulating protein level | Frequent (30-79%) |
| HP:0011123 | Inflammatory abnormality of the skin | Frequent (30-79%) |
| HP:0011227 | Elevated circulating C-reactive protein concentration | Frequent (30-79%) |
| HP:0012649 | Increased inflammatory response | Frequent (30-79%) |
| HP:0030166 | Night sweats | Frequent (30-79%) |
| HP:0031691 | Severe viral infection | Frequent (30-79%) |
| HP:0032018 | Multiple mononeuropathy | Frequent (30-79%) |
| HP:0200029 | Vasculitis in the skin | Frequent (30-79%) |
| HP:0410008 | Abnormality of the peripheral nervous system | Frequent (30-79%) |
| HP:0000093 | Proteinuria | Occasional (5-29%) |
| HP:0000790 | Hematuria | Occasional (5-29%) |
| HP:0000793 | Membranoproliferative glomerulonephritis | Occasional (5-29%) |
| HP:0000822 | Hypertension | Occasional (5-29%) |
| HP:0000965 | Cutis marmorata | Occasional (5-29%) |
| HP:0001063 | Acrocyanosis | Occasional (5-29%) |
| HP:0001369 | Arthritis | Occasional (5-29%) |
| HP:0001482 | Subcutaneous nodule | Occasional (5-29%) |
| HP:0001638 | Cardiomyopathy | Occasional (5-29%) |
| HP:0002011 | Morphological central nervous system abnormality | Occasional (5-29%) |
| HP:0002027 | Abdominal pain | Occasional (5-29%) |
| HP:0002090 | Pneumonia | Occasional (5-29%) |
| HP:0002140 | Ischemic stroke | Occasional (5-29%) |
| HP:0002617 | Dilatation | Occasional (5-29%) |
| HP:0002726 | Recurrent Staphylococcus aureus infections | Occasional (5-29%) |
| HP:0002923 | Rheumatoid factor positive | Occasional (5-29%) |
| HP:0003261 | Increased circulating IgA level | Occasional (5-29%) |
| HP:0003493 | Antinuclear antibody positivity | Occasional (5-29%) |
| HP:0004386 | Gastrointestinal inflammation | Occasional (5-29%) |
| HP:0005318 | Cerebral vasculitis | Occasional (5-29%) |
| HP:0005366 | Recurrent streptococcus pneumoniae infections | Occasional (5-29%) |
| HP:0005401 | Recurrent candida infections | Occasional (5-29%) |
| HP:0006562 | Viral hepatitis | Occasional (5-29%) |
| HP:0006689 | Bacterial endocarditis | Occasional (5-29%) |
| HP:0009830 | Peripheral neuropathy | Occasional (5-29%) |
| HP:0010702 | Increased circulating antibody level | Occasional (5-29%) |
| HP:0011274 | Recurrent mycobacterial infections | Occasional (5-29%) |
| HP:0020101 | Invasive fungal infection | Occasional (5-29%) |
| HP:0020114 | Persistent human papillomavirus infection | Occasional (5-29%) |
| HP:0020180 | Elevated haptoglobin level | Occasional (5-29%) |
| HP:0025143 | Chills | Occasional (5-29%) |
| HP:0025188 | Retinal vasculitis | Occasional (5-29%) |
| HP:0030880 | Raynaud phenomenon | Occasional (5-29%) |
| HP:0031363 | Palpable purpura | Occasional (5-29%) |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | postinfectious vasculitis |
| Mondo ID | MONDO:0018837 |
| Orphanet | 48435 |
| SNOMED CT | 724063005 |
| UMLS | C4510302 |
| MedGen | 1376009 |
| GARD | 0018835 |
| Is cancer (heuristic) | no |
Disease family
This is a subtype of secondary vasculitis. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › cardiovascular disorder › vascular disorder › vasculitis › secondary vasculitis › postinfectious vasculitis
Related subtypes (1): drug-induced vasculitis
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.