Intestinal bleeding
Symptom Information:
Symptom ID: | HPO:0002584 | |||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | ||||||||||||||||||||||||||||||||||||
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) Intestinal bleeding(HPO:0002584) 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 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) Intestinal bleeding(HPO:0002584) Gastrointestinal hemorrhage(HPO:0002239) Intestinal bleeding(HPO:0002584) |
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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) |