Benign lipomatous neoplasm

Summary

Benign lipomatous neoplasm (MONDO:0044983) is a cancer. A subtype of benign connective and soft tissue 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 lipomatous neoplasm
Mondo ID	MONDO:0044983
ICD-10-CM	D17
ICD-11	226447034
NCIT	C4502
UMLS	C0346118
MedGen	91084
Anatomy (UBERON)	UBERON:0001013
Is cancer (heuristic)	yes

Also known as: adipose tissue benign connective and soft tissue neoplasm · benign adipose tissue neoplasm · benign adipose tissue tumor · benign adipose tissue tumour · benign connective and soft tissue neoplasm of adipose tissue · benign lipomatous neoplasm · benign lipomatous tumor · benign lipomatous tumour · benign neoplasm of adipose tissue · benign neoplasm of the adipose tissue · benign tumor of the adipose tissue · benign tumour of adipose tissue · benign tumour of the adipose tissue

Disease family

This is a subtype of benign connective and soft tissue 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 › musculoskeletal system disorder › musculoskeletal system benign neoplasm › benign connective and soft tissue neoplasm › benign lipomatous neoplasm

Related subtypes (4): bone benign neoplasm, benign soft tissue neoplasm, benign osteogenic neoplasm, lipofibromatosis

Subtypes (3): lipoma, lipomatosis, lipoblastoma

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.