Mediastinal neural neoplasm
disease diseaseOn this page
Also known as mediastinal neural tumormediastinal neural tumourmediastinal neurogenic neoplasmmediastinal neurogenic tumormediastinal neurogenic tumourneurogenic neoplasm of mediastinumneurogenic neoplasm of the mediastinumneurogenic tumor of mediastinumneurogenic tumor of the mediastinumneurogenic tumour of mediastinumneurogenic tumour of the mediastinum
Summary
Mediastinal neural neoplasm (MONDO:0003098) is a cancer (an umbrella term covering 5 Mondo subtypes). A subtype of peripheral nervous system neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- Umbrella term: 5 Mondo subtypes
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | mediastinal neural neoplasm |
| Mondo ID | MONDO:0003098 |
| DOID | DOID:4691 |
| NCIT | C6624 |
| UMLS | C1334672 |
| MedGen | 277353 |
| Anatomy (UBERON) | UBERON:0001021, UBERON:0003728 |
| Is cancer (heuristic) | yes |
Also known as: mediastinal neural neoplasm · mediastinal neural tumor · mediastinal neural tumour · mediastinal neurogenic neoplasm · mediastinal neurogenic tumor · mediastinal neurogenic tumour · neurogenic neoplasm of mediastinum · neurogenic neoplasm of the mediastinum · neurogenic tumor of mediastinum · neurogenic tumor of the mediastinum · neurogenic tumour of mediastinum · neurogenic tumour of the mediastinum
Disease family
This is a subtype of peripheral nervous system 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
Related subtypes (8): autonomic nervous system neoplasm, nerve sheath neoplasm, cranial nerve neoplasm, nerve plexus neoplasm, nerve root neoplasm, peripheral ganglioneuroblastoma, peripheral nervous system cancer, benign neoplasm of peripheral nervous system
Subtypes (5): mediastinum neuroblastoma, mediastinum neurofibroma, childhood mediastinal neurogenic neoplasm, mediastinal schwannoma, malignant mediastinal neural neoplasm
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.