Isolated mesenteric vein thrombosis
diseaseOn this page
Summary
Isolated mesenteric vein thrombosis (MONDO:0035009) is a disease. A subtype of thrombotic disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Prevalence: Unknown (Europe) [Orphanet-validated]
- Phenotypes (HPO): 19
Clinical features
Epidemiology
Prevalence records
3 prevalence record(s), Orphanet:
| Type | Class | Value | Geography | Validation |
|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 1.6 | Europe | Validated |
| Annual incidence | 1-9 / 1 000 000 | 0.5 | Finland | Validated |
| Annual incidence | 1-9 / 100 000 | 2.7 | Sweden | Validated |
Signs & symptoms
Clinical features (HPO)
19 HPO clinical features (Orphanet curated; top 19 by frequency):
| HPO ID | Term | Frequency |
|---|---|---|
| HP:0002027 | Abdominal pain | Very frequent (80-99%) |
| HP:0030248 | Mesenteric venous thrombosis | Very frequent (80-99%) |
| HP:0001974 | Leukocytosis | Frequent (30-79%) |
| HP:0002013 | Vomiting | Frequent (30-79%) |
| HP:0002014 | Diarrhea | Frequent (30-79%) |
| HP:0002018 | Nausea | Frequent (30-79%) |
| HP:0002039 | Anorexia | Frequent (30-79%) |
| HP:0001081 | Cholelithiasis | Occasional (5-29%) |
| HP:0001541 | Ascites | Occasional (5-29%) |
| HP:0001945 | Fever | Occasional (5-29%) |
| HP:0002151 | Increased circulating lactate concentration | Occasional (5-29%) |
| HP:0002239 | Gastrointestinal hemorrhage | Occasional (5-29%) |
| HP:0002615 | Hypotension | Occasional (5-29%) |
| HP:0003270 | Abdominal distention | Occasional (5-29%) |
| HP:0030151 | Cholangitis | Occasional (5-29%) |
| HP:0031273 | Shock | Occasional (5-29%) |
| HP:0100806 | Sepsis | Occasional (5-29%) |
| HP:0410282 | Abnormal circulating amylase concentration | Occasional (5-29%) |
| HP:6000377 | Intramural intestinal gas | Occasional (5-29%) |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | isolated mesenteric vein thrombosis |
| Mondo ID | MONDO:0035009 |
| Orphanet | 583861 |
| ICD-11 | 213868120 |
| UMLS | C0267412 |
| MedGen | 120599 |
| GARD | 0022339 |
| Is cancer (heuristic) | no |
Disease family
This is a subtype of thrombotic disease. 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 › thrombotic disease › isolated mesenteric vein thrombosis
Related subtypes (7): marantic endocarditis, portal vein thrombosis, intracranial thrombosis, coronary thrombosis, heparin-induced thrombocytopenia, acquired purpura fulminans, isolated splenic vein thrombosis
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.