Benign neoplasm of pleura

Summary

Benign neoplasm of pleura (MONDO:0021457) 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 pleura
Mondo ID	MONDO:0021457
ICD-11	2142393865
NCIT	C3603
SNOMED CT	92298003
UMLS	C0153955
MedGen	57806
Anatomy (UBERON)	UBERON:0000977
Is cancer (heuristic)	yes

Also known as: benign neoplasm of the pleura · benign pleural neoplasm · benign pleural tumor · benign pleural tumour · benign tumor of pleura · benign tumor of the pleura · benign tumour of pleura · benign tumour of the pleura · pleura 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 pleura

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

Subtypes (2): pleural lipoma, pleural adenomatoid tumor

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.