Gastrointestinal hemorrhage
Symptom Information:
| Symptom ID: | HPO:0002239 | ||||||||||||||||||||||||||||||||||||||||
| Synonyms: |
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| Cross references: |
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| Is a (Direct Parents): |
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| 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 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) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormal bleeding(HPO:0001892) Internal hemorrhage(HPO:0011029) Gastrointestinal hemorrhage(HPO:0002239) MedDRA: Vascular disorders(MedDRA:10047065) Vascular haemorrhagic disorders(MedDRA:10047075) Gastrointestinal hemorrhage(HPO:0002239) |
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| 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) |