Benign neoplasm of oropharynx

Summary

Benign neoplasm of oropharynx (MONDO:0021479) is a cancer. A subtype of respiratory system benign 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	benign neoplasm of oropharynx
Mondo ID	MONDO:0021479
ICD-11	441557450
NCIT	C4604
SNOMED CT	92259008
UMLS	C0347229
MedGen	87572
Anatomy (UBERON)	UBERON:0001729
Is cancer (heuristic)	yes

Also known as: benign neoplasm of the oropharynx · benign oropharyngeal neoplasm · benign oropharyngeal tumor · benign oropharyngeal tumour · benign tumor of oropharynx · benign tumor of the oropharynx · benign tumour of oropharynx · benign tumour of the oropharynx · oropharyngeal neoplasm benign · oropharynx benign neoplasm

Disease family

This is a subtype of respiratory system benign 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 › respiratory system disorder › respiratory system benign neoplasm › benign neoplasm of oropharynx

Related subtypes (14): endobronchial lipoma, benign laryngeal neoplasm, lung benign neoplasm, paranasal sinus Schneiderian papilloma, benign neoplasm of pleura, benign neoplasm of hypopharynx, benign neoplasm of nasal cavity, benign neoplasm of sphenoidal sinus, benign neoplasm of nasopharynx, benign neoplasm of frontal sinus, benign neoplasm of maxillary sinus, benign neoplasm of tonsil, benign neoplasm of ethmoidal sinus, benign neoplasm of trachea

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.