Intestinal bleeding

Symptom Information:

Symptom ID: HPO:0002584
Synonyms:
Gastrointestinal hemorrhage [Orphanet:27600]
Gastrointestinal hemorrhage (disorder) [Orphanet:27600]
Gastrointestinal Hemorrhage [Orphanet:27600]
Intestinal bleeding [OMIM:Intestinal bleeding]
Gastrointestinal bleeding/hemorrhage/hematemesis/melena/rectorrhagia [Orphanet:27600]
Gastrointestinal haemorrhage [Orphanet:27600]
Gastrointestinal haemorrhage [MedDRA:10017955]
Acute on chronic G.I. haemorrhage [MedDRA:10017955]
Bleeding gastrointestinal [MedDRA:10017955]
Gastro intestinal bleed [MedDRA:10017955]
Gastro intestinal bleeding [MedDRA:10017955]
Gastro-intestinal tract bleed [MedDRA:10017955]
Gastrointestinal bleed [MedDRA:10017955]
Gastrointestinal bleeding [MedDRA:10017955]
Gastrointestinal haemorrhage NOS [MedDRA:10017955]
Gastrointestinal hemorrhage [MedDRA:10017955]
Gastrointestinal tract bleed (NOS) [MedDRA:10017955]
Gastrointestinal tract bleed NOS [MedDRA:10017955]
GI bleed [MedDRA:10017955]
GI haemorrhage [MedDRA:10017955]
GI hemorrhage [MedDRA:10017955]
GI tract bleed [MedDRA:10017955]
Haemorrhage of digestive tract [MedDRA:10017955]
Haemorrhage of gastrointestinal tract, unspecified [MedDRA:10017955]
Hemorrhage gastrointestinal [MedDRA:10017955]
Hemorrhage of gastrointestinal tract, unspecified [MedDRA:10017955]
Hemorrhage of digestive tract [MedDRA:10017955]
Haemorrhage gastrointestinal [MedDRA:10017955]
GI hemorrhage (onset usually in 5th -6th decade) [OMIM:GI hemorrhage (onset usually in 5th -6th decade)]
Gastrointestinal hemorrhage (onset usually 5th-6th decade) [OMIM:Gastrointestinal hemorrhage (onset usually 5th-6th decade)]
Rectal haemorrhage [MedDRA:10038063]
Rectorrhagia [Orphanet:27600]
Rectal hemorrhage (disorder) [Orphanet:27600]
Rectal hemorrhage [Orphanet:27600]
Gastrointestinal haemorrhages [MedDRA:10052742]
Quality:
Cross references:
HPO:0002239 "Gastrointestinal hemorrhage" [Orphanet:27600]
Orphanet:27600 "Gastrointestinal bleeding/hemorrhage/hematemesis/melena/rectorrhagia" [Orphanet:27600]
OMIM: "Intestinal bleeding" [OMIM:Intestinal bleeding]
OMIM: "GI hemorrhage (onset usually in 5th -6th decade)" [OMIM:GI hemorrhage (onset usually in 5th -6th decade)]
OMIM: "Gastrointestinal hemorrhage (onset usually 5th-6th decade)" [OMIM:Gastrointestinal hemorrhage (onset usually 5th-6th decade)]
UMLS:C0017181 "Gastrointestinal Hemorrhage" [Orphanet:27600]
UMLS:C0267596 "Rectal hemorrhage" [Orphanet:27600]
Is a (Direct Parents):
HPO         Small intestinal bleeding
HPO         Gastrointestinal hemorrhage
MedDRA Gastrointestinal hemorrhage
Orphanet Functional anomalies of the digestive system
MedDRA Vascular haemorrhagic disorders
Orphanet Gastrointestinal hemorrhage
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Internal hemorrhage(HPO:0011029)
                Gastrointestinal hemorrhage(HPO:0002239)
                   Intestinal bleeding(HPO:0002584)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Gastrointestinal hemorrhage(HPO:0002239)
                   Intestinal bleeding(HPO:0002584)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of cardiovascular system physiology(HPO:0011025)
             Abnormality of blood circulation(HPO:0011028)
                Internal hemorrhage(HPO:0011029)
                   Gastrointestinal hemorrhage(HPO:0002239)
                      Intestinal bleeding(HPO:0002584)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular haemorrhagic disorders(MedDRA:10047075)
       Gastrointestinal hemorrhage(HPO:0002239)
          Intestinal bleeding(HPO:0002584)
       Intestinal bleeding(HPO:0002584)
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

BLEEDING DISORDER, PLATELET-TYPE, 12 (OMIM:605735)
Blue rubber bleb nevus (Orphanet:1059)
COLONIC VARICES WITHOUT PORTAL HYPERTENSION (OMIM:120440)
Coats plus syndrome (Orphanet:313838)
FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF (OMIM:134430)
Gaucher disease type 2 (Orphanet:77260)
Hereditary fructose intolerance (Orphanet:469)
Lymphangioleiomyomatosis (Orphanet:538)
Menkes disease (Orphanet:565)
Mucocutaneous venous malformations (Orphanet:2451)
PHOSPHOLIPASE A2, GROUP IVA (OMIM:600522)
Peutz-Jeghers syndrome (Orphanet:2869)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
Tyrosinemia type 1 (Orphanet:882)
Wolfram syndrome (Orphanet:3463)