Hematochezia

Symptom Information:

Symptom ID: HPO:0002573
Synonyms:
Bloody diarrhea [HPO:0002573]
Rectal bleeding [HPO:0002573]
RECURRENT RECTAL BLEEDING [HPO:0002573]
Haematochezia [HPO:0002573]
Bloody diarrhea [OMIM:Bloody diarrhea]
Hematochezia [OMIM:Hematochezia]
Rectal bleeding [OMIM:Rectal bleeding]
Recurrent rectal bleeding [OMIM:Recurrent rectal bleeding]
Diarrhea, bloody [OMIM:Diarrhea, bloody]
Haematochezia [MedDRA:10018836]
Quality:
Cross references:
OMIM: "Bloody diarrhea" [OMIM:Bloody diarrhea]
OMIM: "Hematochezia" [OMIM:Hematochezia]
OMIM: "Rectal bleeding" [OMIM:Rectal bleeding]
OMIM: "Recurrent rectal bleeding" [OMIM:Recurrent rectal bleeding]
OMIM: "Diarrhea, bloody" [OMIM:Diarrhea, bloody]
UMLS:C0018932 "Haematochezia" [HPO:0002573]
Is a (Direct Parents):
MedDRA Gastrointestinal hemorrhage
HPO         Gastrointestinal hemorrhage
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)
                      Hematochezia(HPO:0002573)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Gastrointestinal hemorrhage(HPO:0002239)
                   Hematochezia(HPO:0002573)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Internal hemorrhage(HPO:0011029)
                Gastrointestinal hemorrhage(HPO:0002239)
                   Hematochezia(HPO:0002573)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular haemorrhagic disorders(MedDRA:10047075)
       Gastrointestinal hemorrhage(HPO:0002239)
          Hematochezia(HPO:0002573)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Cronkhite-Canada syndrome (Orphanet:2930)
ENTEROCOLITIS (OMIM:226150)
Generalized juvenile polyposis/juvenile polyposis coli (Orphanet:329971)
HERMANSKY-PUDLAK SYNDROME 1 (OMIM:203300)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
INFLAMMATORY BOWEL DISEASE 11 (OMIM:191390)
INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE (OMIM:613148)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (OMIM:175050)
Juvenile polyposis syndrome (Orphanet:2929)
Multiple intestinal atresia (Orphanet:2300)
Neonatal inflammatory skin and bowel disease (Orphanet:294023)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
WISKOTT-ALDRICH SYNDROME (OMIM:277970)
Wiskott-Aldrich syndrome (Orphanet:906)