Nerve root neoplasm

Summary

Nerve root neoplasm (MONDO:0003103) 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 root neoplasm
Mondo ID	MONDO:0003103
DOID	DOID:4698
NCIT	C5119
UMLS	C1334946
MedGen	233753
Anatomy (UBERON)	UBERON:0002211
Is cancer (heuristic)	yes

Also known as: neoplasm of nerve Root · neoplasm of nerve root · neoplasm of the nerve Root · neoplasms, nerve Root · nerve root neoplasm (disease) · nerve Root neoplasms · nerve Root tumor · nerve root tumor · nerve Root tumors · nerve Root tumour · nerve root tumour · nerve Root tumours · tumor of nerve Root · tumor of nerve root · tumor of the nerve Root · tumour of nerve Root · tumour of nerve root · tumour of the nerve Root

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 root neoplasm

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

Subtypes (1): cauda equina 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.