Gastrointestinal infarctions

Symptom Information:

Symptom ID: HPO:0005244
Synonyms:
Visceral ischemia syndrome [Orphanet:35780]
Mesenteric infarction (disorder) [Orphanet:35780]
Mesenteric infarction [Orphanet:35780]
Intestinal infarction [Orphanet:35780]
Gastrointestinal infarctions [OMIM:Gastrointestinal infarctions]
Mesenteric/intestinal infarction [Orphanet:35780]
Infarction mesenteric [Orphanet:35780]
Intestinal infarction [MedDRA:10022657]
Bowel infarction [MedDRA:10022657]
Infarction mesenteric [MedDRA:10022657]
Intestinal infarct [MedDRA:10022657]
Quality:
Cross references:
Orphanet:35780 "Mesenteric/intestinal infarction" [Orphanet:35780]
OMIM: "Gastrointestinal infarctions" [OMIM:Gastrointestinal infarctions]
UMLS:C0267406 "Mesenteric infarction" [Orphanet:35780]
UMLS:C0241950 "Intestinal infarction" [Orphanet:35780]
Is a (Direct Parents):
Orphanet Acute ischemic syndrome
HPO         Abnormality of the gastrointestinal tract
MedDRA Gastrointestinal vascular occlusion and infarction
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Gastrointestinal infarctions(HPO:0005244)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Gastrointestinal vascular conditions(MedDRA:10018031)
       Gastrointestinal vascular occlusion and infarction(MedDRA:10017997)
          Gastrointestinal infarctions(HPO:0005244)
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Blue rubber bleb nevus (Orphanet:1059)
Budd-Chiari syndrome (Orphanet:131)
Cryoglobulinemic vasculitis (Orphanet:91138)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Familial Mediterranean fever (Orphanet:342)
Giant cell arteritis (Orphanet:397)
Immunoglobulin A vasculitis (Orphanet:761)
Malignant atrophic papulosis (Orphanet:679)
Microscopic polyangiitis (Orphanet:727)
Peutz-Jeghers syndrome (Orphanet:2869)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Secondary polycythemia (Orphanet:98428)
Takayasu arteritis (Orphanet:3287)