Celiac trunk compression syndrome

Summary

Celiac trunk compression syndrome (MONDO:0017388) is a disease and 2 clinical trials. A subtype of arterial disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Prevalence: Unknown (Worldwide)
• Clinical trials: 2

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	celiac trunk compression syndrome
Mondo ID	MONDO:0017388
MeSH	C566151
OMIM	116870
Orphanet	293208
DOID	DOID:9892
ICD-10-CM	I77.4
ICD-11	1666443751
SNOMED CT	9250002
GARD	0012308
NORD	1957
Is cancer (heuristic)	no

Also known as: celiac access syndrome · celiac artery compression syndrome · celiac artery stenosis from compression by median arcuate ligament of diaphragm · coeliac access syndrome · coeliac artery compression syndrome · Dunbar syndrome · Median Arcuate Ligament Syndrome · median arcuate ligament syndrome · median arcuate ligament syndromic disease · syndromic disease of median arcuate ligament

Disease family

This is a subtype of arterial disorder. 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 › cardiovascular disorder › vascular disorder › arterial disorder › celiac trunk compression syndrome

Related subtypes (29): vertebral artery insufficiency, splenic artery aneurysm, basilar artery insufficiency, arteriosclerosis disorder, subclavian artery aneurysm, pulmonary artery choriocarcinoma, pulmonary artery leiomyosarcoma, coronary artery disorder, hypertensive disorder, carotid artery disorder, pulmonary embolism, peripheral arterial disease, hypotensive disorder, large artery stroke, aortic disorder, cervical artery dissection, anterior spinal artery syndrome, fibromuscular dysplasia, retinal arterial tortuosity, Sneddon syndrome, pediatric arterial ischemic stroke, absence of the pulmonary artery, arterial occlusion, aberrant subclavian artery, anterior spinal artery stroke, arteritis, pulmonary artery disease, fibromuscular dysplasia, multifocal, carotid web

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
NCT05468580	Not specified	RECRUITING	Coeliac Artery Release or Sham Operation
NCT06468774	Not specified	RECRUITING	Intestinal Ischemia Biomarker in Patients With Chronic Mesenteric Ischemia