Autonomic nervous system neoplasm
disease diseaseOn this page
Also known as autonomic nervous system neoplasm (disease)autonomic nervous system neoplasmsautonomic nervous system tumorautonomic nervous system tumourneoplasm of autonomic nervous systemneoplasm of the autonomic nervous systemtumor of autonomic nervous systemtumor of the autonomic nervous systemtumour of autonomic nervous systemtumour of the autonomic nervous system
Summary
Autonomic nervous system neoplasm (MONDO:0002366) is a cancer. A subtype of autonomic nervous system disorder — 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 | autonomic nervous system neoplasm |
| Mondo ID | MONDO:0002366 |
| DOID | DOID:2621 |
| NCIT | C5112 |
| UMLS | C1332356 |
| MedGen | 231389 |
| Anatomy (UBERON) | UBERON:0002410 |
| Is cancer (heuristic) | yes |
Also known as: autonomic nervous system neoplasm · autonomic nervous system neoplasm (disease) · autonomic nervous system neoplasms · autonomic nervous system tumor · autonomic nervous system tumour · neoplasm of autonomic nervous system · neoplasm of the autonomic nervous system · tumor of autonomic nervous system · tumor of the autonomic nervous system · tumour of autonomic nervous system · tumour of the autonomic nervous system
Disease family
This is a subtype of autonomic nervous system disorder. 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 › central nervous system disorder › autonomic nervous system disorder › autonomic nervous system neoplasm
Related subtypes (12): idiopathic peripheral autonomic neuropathy, autonomic neuropathy, Frey syndrome, harlequin syndrome, chronic hiccup, pure autonomic failure, baroreflex failure, autonomic dysreflexia, dysautonomia, sympathetic nervous system disorder, parasympathetic nervous system disorder, central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease
Subtypes (3): paraganglioma, sympathetic neurilemmoma, ganglioneuroma
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.