Ethmoid sinus ectopic meningioma
disease diseaseOn this page
Also known as ethmoid sinus primary ectopic meningiomaethmoidal sinus primary ectopic meningiomaprimary ectopic meningioma of ethmoid sinusprimary ectopic meningioma of ethmoidal sinusprimary ectopic meningioma of the ethmoid sinusprimary ectopic meningioma of the ethmoidal sinus
Summary
Ethmoid sinus ectopic meningioma (MONDO:0004014) is a disease. A subtype of ethmoidal sinus neoplasm — 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 | ethmoid sinus ectopic meningioma |
| Mondo ID | MONDO:0004014 |
| DOID | DOID:6854 |
| NCIT | C5309 |
| UMLS | C1333475 |
| MedGen | 232473 |
| GARD | 0023776 |
| Is cancer (heuristic) | no |
Also known as: ethmoid sinus primary ectopic meningioma · ethmoidal sinus primary ectopic meningioma · primary ectopic meningioma of ethmoid sinus · primary ectopic meningioma of ethmoidal sinus · primary ectopic meningioma of the ethmoid sinus · primary ectopic meningioma of the ethmoidal sinus
Disease family
Classification path: disease › human disease › disease by body system or component › otorhinolaryngologic disease › nasal disorder › paranasal sinus disorder › paranasal sinus neoplasm › ethmoidal sinus neoplasm › ethmoid sinus ectopic meningioma
Related subtypes (2): ethmoid sinus cancer, benign neoplasm of ethmoidal sinus
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.