Hematemesis
Symptom Information:
Symptom ID: | HPO:0002248 | ||||||||||||||||||||||
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 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) Hematemesis(HPO:0002248) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Gastrointestinal hemorrhage(HPO:0002239) Hematemesis(HPO:0002248) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormal bleeding(HPO:0001892) Internal hemorrhage(HPO:0011029) Gastrointestinal hemorrhage(HPO:0002239) Hematemesis(HPO:0002248) MedDRA: Vascular disorders(MedDRA:10047065) Vascular haemorrhagic disorders(MedDRA:10047075) Gastrointestinal hemorrhage(HPO:0002239) Hematemesis(HPO:0002248) |
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Database Frequency: | 12 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Menkes disease | (Orphanet:565) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Neonatal hemochromatosis | (Orphanet:446) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER | (OMIM:187300) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
Wolfram syndrome | (Orphanet:3463) |