Nerve plexus neoplasm

Summary

Nerve plexus neoplasm (MONDO:0003100) is a cancer. 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

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	nerve plexus neoplasm
Mondo ID	MONDO:0003100
DOID	DOID:4693
NCIT	C5822
UMLS	C1334945
MedGen	235366
GARD	0023368
Anatomy (UBERON)	UBERON:0001810
Is cancer (heuristic)	yes

Also known as: neoplasm of nerve plexus · neoplasm of the nerve plexus · nerve plexus neoplasm · nerve plexus neoplasm (disease) · nerve plexus neoplasms · nerve plexus tumor · nerve plexus tumors · nerve plexus tumour · nerve plexus tumours · neural plexus neoplasms · neural plexus tumors · neural plexus tumours · tumor of nerve plexus · tumor of the nerve plexus · tumour of nerve plexus · tumour of the nerve plexus

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 › nerve plexus neoplasm

Related subtypes (8): autonomic nervous system neoplasm, nerve sheath neoplasm, cranial nerve neoplasm, mediastinal neural neoplasm, nerve root neoplasm, peripheral ganglioneuroblastoma, peripheral nervous system cancer, benign neoplasm of peripheral nervous system

Subtypes (2): brachial plexus neoplasm, lumbar plexus 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.