Mediastinum neurofibroma

Summary

Mediastinum neurofibroma (MONDO:0001426) 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	mediastinum neurofibroma
Mondo ID	MONDO:0001426
DOID	DOID:12064
NCIT	C6631
UMLS	C1334674
MedGen	277354
GARD	0022943
Anatomy (UBERON)	UBERON:0003728
Is cancer (heuristic)	no

Also known as: mediastinal neurofibroma · mediastinum neurofibroma · neurofibroma of mediastinum · neurofibroma 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 › mediastinum neurofibroma

Related subtypes (4): mediastinum neuroblastoma, 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.