Intestinal benign neoplasm

Summary

Intestinal benign neoplasm (MONDO:0003062) is a cancer. A subtype of benign digestive 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	intestinal benign neoplasm
Mondo ID	MONDO:0003062
NCIT	C4609
SNOMED CT	92151003
UMLS	C0347269
MedGen	91124
Anatomy (UBERON)	UBERON:0000160
Is cancer (heuristic)	yes

Also known as: benign intestinal neoplasm · benign intestinal neoplasms · benign intestinal tumor · benign intestinal tumors · benign intestinal tumour · benign intestinal tumours · benign intestine neoplasm · benign intestine tumor · benign intestine tumour · benign neoplasm of intestines · benign neoplasm of the intestines · benign neoplasms of large and/or small intestine · benign neoplasms of the large and/or small intestine · benign tumor of intestines · benign tumor of the intestines · benign tumour of intestines · benign tumour of the intestines · intestinal neoplasms, benign · intestinal tumors, benign · intestine benign neoplasm

Disease family

This is a subtype of benign digestive 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 › digestive system disorder › benign digestive system neoplasm › intestinal benign neoplasm

Related subtypes (9): bile duct papillary neoplasm, pleomorphic adenoma, hepatocellular adenoma, benign neoplasm of stomach, benign neoplasm of esophagus, benign neoplasm of pancreas, benign neoplasm of oropharynx, benign neoplasm of gallbladder, hepatobiliary benign neoplasm

Subtypes (2): benign neoplasm of large intestine, benign neoplasm of small intestine

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.