Liver angiosarcoma
diseaseOn this page
Also known as angiosarcoma (disease) of liverangiosarcoma of liverangiosarcoma of the liverhemangiosarcoma of liverhemangiosarcoma of the liverhepatic angiosarcomahepatic hemangiosarcomaLiasliver angiosarcoma (disease)liver hemangiosarcomaprimary angiosarcoma of liverprimary angiosarcoma of the liver
Summary
Liver angiosarcoma (MONDO:0002387) is a disease and 2 clinical trials. A subtype of liver sarcoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 2
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | liver angiosarcoma |
| Mondo ID | MONDO:0002387 |
| DOID | DOID:268 |
| ICD-10-CM | C22.3 |
| ICD-11 | 965491615 |
| NCIT | C4438 |
| SNOMED CT | 109844006 |
| UMLS | C0345907 |
| MedGen | 138027 |
| GARD | 0005813 |
| Anatomy (UBERON) | UBERON:0002107 |
| Is cancer (heuristic) | no |
Also known as: angiosarcoma (disease) of liver · angiosarcoma of liver · angiosarcoma of the liver · hemangiosarcoma of liver · hemangiosarcoma of the liver · hepatic angiosarcoma · hepatic hemangiosarcoma · Lias · liver angiosarcoma · liver angiosarcoma (disease) · liver hemangiosarcoma · primary angiosarcoma of liver · primary angiosarcoma of the liver
Data availability: 1 cell line.
Disease family
This is a subtype of liver sarcoma. 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 › digestive system cancer › liver cancer › liver sarcoma › liver angiosarcoma
Related subtypes (6): liver rhabdomyosarcoma, bile duct sarcoma, liver leiomyosarcoma, liver extraskeletal osteosarcoma, liver fibrosarcoma, undifferentiated (embryonal) sarcoma
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: 2.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06541652 | Not specified | RECRUITING | A French Multicenter Observational Retrospective Study of Rare Primary Liver Cancers |
| NCT03025438 | Not specified | COMPLETED | Cytological Diagnosis of Hepatic Angiosarcoma and Its Histopathologic Correlation |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.