Post-infectious disorder
diseaseOn this page
Also known as sequela of infectious disorder
Summary
Post-infectious disorder (MONDO:0021669) is a disease (an umbrella term covering 14 Mondo subtypes) and 2 clinical trials. A subtype of disease of primarily extrinsic mechanism — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Umbrella term: 14 Mondo subtypes
- Clinical trials: 2
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | post-infectious disorder |
| Mondo ID | MONDO:0021669 |
| ICD-10-CM | B90-B94 |
| SNOMED CT | 123976001 |
| UMLS | C1264603 |
| MedGen | 688819 |
| Is cancer (heuristic) | no |
Also known as: sequela of infectious disorder
Disease family
An umbrella term covering 14 Mondo subtypes.
Classification path: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › post-infectious disorder
Related subtypes (6): infectious disease, poisoning, radiation-induced disorder, iatrogenic disease, occupational disorder, disease related to transplantation
Subtypes (14): encephalopathy, acute, infection-induced, infective urethral stricture, infectious otitis interna, otitis externa, infected hydrocele, Chagas cardiomyopathy, postinfectious vasculitis, postinfectious encephalitis, post-infectious syndrome, post-bacterial disorder, post-viral disorder, infection-related hemolytic uremic syndrome, infectious neuropathy, infection-induced acute-onset axonal neuropathy
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: 2.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE1/PHASE2 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04846010 | PHASE1/PHASE2 | UNKNOWN | Recovering Damaged Cells for Sequelae Caused by COVID-19, SARS-CoV-2 |
| NCT06085911 | Not specified | UNKNOWN | RCT Long COVID-19 Rehabilitation |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.