Diaphragma sellae meningioma
disease diseaseOn this page
Also known as diaphragm sellae meningiomadiaphragma sellae meningioma (disease)meningioma (disease) of diaphragma sellaemeningioma of diaphragm sellaemeningioma of Diaphragma sellaemeningioma of the diaphragm sellaemeningioma of the Diaphragma sellae
Summary
Diaphragma sellae meningioma (MONDO:0004108) is a disease and 1 clinical trial. Top therapeutic interventions include bupivacaine and prilocaine. A subtype of sella turcica neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 1
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | diaphragma sellae meningioma |
| Mondo ID | MONDO:0004108 |
| DOID | DOID:7103 |
| NCIT | C5283 |
| UMLS | C1333283 |
| MedGen | 234200 |
| GARD | 0023829 |
| Anatomy (UBERON) | UBERON:0035416 |
| Is cancer (heuristic) | no |
Also known as: diaphragm sellae meningioma · diaphragma sellae meningioma (disease) · meningioma (disease) of diaphragma sellae · meningioma of diaphragm sellae · meningioma of Diaphragma sellae · meningioma of the diaphragm sellae · meningioma of the Diaphragma sellae
Disease family
Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › head and neck neoplasm › skull neoplasm › skull base neoplasm › sella turcica neoplasm › diaphragma sellae meningioma
Related subtypes (3): tuberculum sellae meningioma, pituitary tumor, craniopharyngioma
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: 1.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE4 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04756050 | PHASE4 | COMPLETED | Comparison of Different Approaches for Supraclavicular Block and Their Effects on Diaphragm Muscle Function |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| BUPIVACAINE | 4 | 1 |
| PRILOCAINE | 4 | 1 |
Related Atlas pages
- Drugs: Bupivacaine, Prilocaine