Hematemesis

Symptom Information:

Symptom ID: HPO:0002248
Synonyms:
Blood in vomit - symptom (finding) [Orphanet:27600]
Hematemesis (disorder) [Orphanet:27600]
HAEMATEMESIS [HPO:0002248]
Hematemesis [Orphanet:27600]
Hematemesis [OMIM:Hematemesis]
Gastrointestinal bleeding/hemorrhage/hematemesis/melena/rectorrhagia [Orphanet:27600]
Haematemesis [Orphanet:27600]
Haematemesis [MedDRA:10018830]
Blood clot discharge [MedDRA:10018830]
Coffee ground vomiting [MedDRA:10018830]
Emesis bloody [MedDRA:10018830]
Hematemesis [MedDRA:10018830]
Large haematemesis [MedDRA:10018830]
Massive haematemesis [MedDRA:10018830]
Vomiting blood [MedDRA:10018830]
Coffee ground emesis [MedDRA:10018830]
Large hematemesis [MedDRA:10018830]
Massive hematemesis [MedDRA:10018830]
Rectal haemorrhage [MedDRA:10038063]
Rectorrhagia [Orphanet:27600]
Rectal hemorrhage (disorder) [Orphanet:27600]
Rectal hemorrhage [Orphanet:27600]
Quality:
Cross references:
Orphanet:27600 "Gastrointestinal bleeding/hemorrhage/hematemesis/melena/rectorrhagia" [Orphanet:27600]
OMIM: "Hematemesis" [OMIM:Hematemesis]
UMLS:C0018926 "HAEMATEMESIS" [HPO:0002248]
UMLS:C0018926 "Hematemesis" [Orphanet:27600]
UMLS:C0267596 "Rectal hemorrhage" [Orphanet:27600]
Is a (Direct Parents):
Orphanet Gastrointestinal hemorrhage
MedDRA Gastrointestinal hemorrhage
Orphanet Functional anomalies of the digestive system
HPO         Gastrointestinal hemorrhage
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)
                   Hematemesis(HPO:0002248)
       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 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)
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)