Gastrointestinal hemorrhage

Symptom Information:

Symptom ID: HPO:0002239
Synonyms:
Gastrointestinal bleeding [HPO:0002239]
GI haemorrhage [HPO:0002239]
GI hemorrhage [HPO:0002239]
Gastrointestinal hemorrhage (disorder) [Orphanet:27600]
Gastrointestinal Hemorrhage [Orphanet:27600]
GI hemorrhage [OMIM:GI hemorrhage]
Gastrointestinal bleeding [OMIM:Gastrointestinal bleeding]
Gastrointestinal hemorrhage [OMIM:Gastrointestinal hemorrhage]
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]
GI bleeding [OMIM,du]
Quality:
Cross references:
HPO:0002584 "Intestinal bleeding" [Orphanet:27600]
Orphanet:27600 "Gastrointestinal bleeding/hemorrhage/hematemesis/melena/rectorrhagia" [Orphanet:27600]
OMIM: "GI hemorrhage" [OMIM:GI hemorrhage]
OMIM: "Gastrointestinal bleeding" [OMIM:Gastrointestinal bleeding]
OMIM: "Gastrointestinal hemorrhage" [OMIM:Gastrointestinal hemorrhage]
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         Internal hemorrhage
MedDRA Vascular haemorrhagic disorders
Orphanet Functional anomalies of the digestive system
HPO         Abnormality of the gastrointestinal tract
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 hemorrhage(HPO:0002239)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Internal hemorrhage(HPO:0011029)
                Gastrointestinal hemorrhage(HPO:0002239)
       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)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular haemorrhagic disorders(MedDRA:10047075)
       Gastrointestinal hemorrhage(HPO:0002239)
Database Frequency: 97 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
Adams-Oliver syndrome (Orphanet:974)
Alström syndrome (Orphanet:64)
Alveolar echinococcosis (Orphanet:284)
Angio-osteohypertrophic syndrome (Orphanet:2346)
BLEEDING DISORDER, PLATELET-TYPE, 12 (OMIM:605735)
BLEEDING DISORDER, PLATELET-TYPE, 17 (OMIM:187900)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Behçet disease (Orphanet:117)
Blue rubber bleb nevus (Orphanet:1059)
Budd-Chiari syndrome (Orphanet:131)
CEDNIK syndrome (Orphanet:66631)
CREST syndrome (Orphanet:90290)
Carney triad (Orphanet:139411)
Carney-Stratakis syndrome (Orphanet:97286)
Cholestasis - lymphedema (Orphanet:1414)
Chédiak-Higashi syndrome (Orphanet:167)
Classical homocystinuria (Orphanet:394)
Cogan syndrome (Orphanet:1467)
Congenital bile acid synthesis defect type 1 (Orphanet:79301)
Congenital bile acid synthesis defect type 3 (Orphanet:79302)
Congenital factor II deficiency (Orphanet:325)
Congenital factor X deficiency (Orphanet:328)
Cowden syndrome (Orphanet:201)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Cronkhite-Canada syndrome (Orphanet:2930)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cutaneous mastocytosis (Orphanet:66646)
Dengue fever (Orphanet:99828)
Desmoid tumor (Orphanet:873)
Diffuse cutaneous mastocytosis (Orphanet:79456)
EPSTEIN SYNDROME (OMIM:153650)
Ebola hemorrhagic fever (Orphanet:319218)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Familial dysfibrinogenemia (Orphanet:98881)
Familial hypofibrinogenemia (Orphanet:101041)
GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA (OMIM:137560)
Gastrointestinal stromal tumor (Orphanet:44890)
Glanzmann thrombasthenia (Orphanet:849)
Granulomatosis with polyangiitis (Orphanet:900)
HEMOPHILIA A WITH VASCULAR ABNORMALITY (OMIM:306800)
Hemophilia B (Orphanet:98879)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Hereditary fructose intolerance (Orphanet:469)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hereditary mixed polyposis syndrome (Orphanet:157794)
Hereditary neurocutaneous angioma (Orphanet:1062)
Hereditary nonpolyposis colon cancer (Orphanet:144)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hydatidosis (Orphanet:400)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
INTEGRIN, BETA-3 (OMIM:173470)
Immunoglobulin A vasculitis (Orphanet:761)
Isolated polycystic liver disease (Orphanet:2924)
Juvenile dermatomyositis (Orphanet:93672)
Juvenile polyposis syndrome (Orphanet:2929)
Klippel-Trénaunay syndrome (Orphanet:90308)
Lassa fever (Orphanet:99824)
Lujo hemorrhagic fever (Orphanet:319213)
Lyell syndrome (Orphanet:537)
Lymphangioleiomyomatosis (Orphanet:538)
Malignant atrophic papulosis (Orphanet:679)
Marburg hemorrhagic fever (Orphanet:99826)
Mastocytosis (Orphanet:98292)
Menetrier disease (Orphanet:2494)
Menkes disease (Orphanet:565)
Microscopic polyangiitis (Orphanet:727)
Mixed connective tissue disease (Orphanet:809)
Neonatal hemochromatosis (Orphanet:446)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Non-polyposis Turcot syndrome (Orphanet:99817)
PLASMA CLOT RETRACTION FACTOR, DEFICIENCY OF (OMIM:262800)
PSEUDOXANTHOMA ELASTICUM, FORME FRUSTEPSEUDOXANTHOMA ELASTICUM, HETEROZYGOUS, INCLUDED (OMIM:177850)
Pachydermoperiostosis (Orphanet:2796)
Palmoplantar keratoderma-esophageal carcinoma syndrome (Orphanet:2198)
Peutz-Jeghers syndrome (Orphanet:2869)
Polyarteritis nodosa (Orphanet:767)
Polycythemia vera (Orphanet:729)
Polymyositis (Orphanet:732)
Pseudoxanthoma elasticum (Orphanet:758)
Reynolds syndrome (Orphanet:779)
Rift valley fever (Orphanet:319251)
Scleroderma (Orphanet:801)
Stevens-Johnson syndrome (Orphanet:36426)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
Typhoid (Orphanet:99745)
Tyrosinemia type 1 (Orphanet:882)
Viral hemorrhagic fever (Orphanet:341)
Von Willebrand disease type 1 (Orphanet:166078)
Waldenström macroglobulinemia (Orphanet:33226)
Whipple disease (Orphanet:3452)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 2 (OMIM:604928)
Yellow fever (Orphanet:99829)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)