Mediastinal schwannoma
disease diseaseOn this page
Also known as benign mediastinal neurilemmomabenign mediastinal schwannomabenign neurilemmoma of mediastinumbenign neurilemmoma of the mediastinumbenign schwannoma of mediastinumbenign schwannoma of the mediastinummediastinal neurilemmomamediastinum schwannomaneurilemmoma of mediastinumneurilemmoma of the mediastinumschwannoma of mediastinumschwannoma of the mediastinum
Summary
Mediastinal schwannoma (MONDO:0004398) is a disease. A subtype of mediastinal neural 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 | mediastinal schwannoma |
| Mondo ID | MONDO:0004398 |
| DOID | DOID:6175, DOID:7922 |
| NCIT | C6643 |
| UMLS | C1334679 |
| MedGen | 233688 |
| GARD | 0023978 |
| Anatomy (UBERON) | UBERON:0003728 |
| Is cancer (heuristic) | no |
Also known as: benign mediastinal neurilemmoma · benign mediastinal schwannoma · benign neurilemmoma of mediastinum · benign neurilemmoma of the mediastinum · benign schwannoma of mediastinum · benign schwannoma of the mediastinum · mediastinal neurilemmoma · mediastinal schwannoma · mediastinum schwannoma · neurilemmoma of mediastinum · neurilemmoma of the mediastinum · schwannoma of mediastinum · schwannoma of the mediastinum
Disease family
This is a subtype of mediastinal neural neoplasm. 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 › nervous system disorder › peripheral nervous system disorder › peripheral nervous system neoplasm › mediastinal neural neoplasm › mediastinal schwannoma
Related subtypes (4): mediastinum neuroblastoma, mediastinum neurofibroma, childhood mediastinal neurogenic neoplasm, malignant mediastinal neural neoplasm
Subtypes (1): benign mediastinal psammomatous neurilemmoma
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.