Bone angiosarcoma

Summary

Bone angiosarcoma (MONDO:0002617) is a disease and 1 clinical trial. A subtype of angiosarcoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Clinical trials: 1

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	bone angiosarcoma
Mondo ID	MONDO:0002617
DOID	DOID:3351
NCIT	C6479
UMLS	C1332574
MedGen	231448
GARD	0023189
Anatomy (UBERON)	UBERON:0002481
Is cancer (heuristic)	no

Also known as: angiosarcoma (disease) of bone tissue · bone angioendothelial sarcoma · bone angiosarcoma · bone Hemangioendothelial sarcoma · bone hemangiosarcoma · bone tissue angiosarcoma (disease) · osseous angioendothelial sarcoma · osseous angiosarcoma · osseous hemangiosarcoma

Disease family

This is a subtype of angiosarcoma. 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 etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › cardiovascular cancer › vascular cancer › angiosarcoma › bone angiosarcoma

Related subtypes (18): spleen angiosarcoma, liver angiosarcoma, central nervous system angiosarcoma, pediatric angiosarcoma, aorta angiosarcoma, breast angiosarcoma, conventional angiosarcoma, gallbladder angiosarcoma, thyroid gland angiosarcoma, skin angiosarcoma, superior vena cava angiosarcoma, prostate angiosarcoma, mediastinum angiosarcoma, ovarian angiosarcoma, pulmonary vein leiomyosarcoma, pulmonary artery leiomyosarcoma, Kaposi’s sarcoma, angiosarcoma of the scalp

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: 1.

Phase distribution (across all retrieved trials)

Phase	Trials
Not specified	1

Top trials by phase / activity

NCT	Phase	Status	Title
NCT05515068	Not specified	NOT_YET_RECRUITING	Registry For Children, Adolescents And Adults With Osteosarcoma And Biologically Related Bone Sarcomas