Ergotism
disease diseaseOn this page
Also known as ergot poisoningergot poisoningsergotismsfire, St. Anthonyspoisoning, ergotpoisonings, ergotSaint Anthony fireSaint Anthony's fireSaint Anthonys fireSt Anthony's fireSt. Anthony fireSt. Anthony's fireSt. Anthonys fire
Summary
Ergotism (MONDO:0042496) is a disease. A subtype of mycotoxicosis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | ergotism |
| Mondo ID | MONDO:0042496 |
| MeSH | D004881 |
| ICD-11 | 1013848192 |
| SNOMED CT | 51510002 |
| Is cancer (heuristic) | no |
Also known as: ergot poisoning · ergot poisonings · ergotism · ergotisms · fire, St. Anthonys · poisoning, ergot · poisonings, ergot · Saint Anthony fire · Saint Anthony’s fire · Saint Anthonys fire · St Anthony’s fire · St. Anthony fire · St. Anthony’s fire · St. Anthonys fire
Disease family
This is a subtype of mycotoxicosis. 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 etiologic mechanism › disease of primarily extrinsic mechanism › infectious disease › fungal infectious disease › mycotoxicosis › ergotism
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.