Melena

Symptom Information:

Symptom ID: HPO:0002249
Synonyms:
Dark stools (finding) [Orphanet:27600]
Melena due to gastrointestinal hemorrhage (disorder) [Orphanet:27600]
Melena (disorder) [Orphanet:27600]
melena [HPO:0002249]
Feces color: tarry [Orphanet:27600]
Melena [Orphanet:27600]
Melena [OMIM:Melena]
Gastrointestinal bleeding/hemorrhage/hematemesis/melena/rectorrhagia [Orphanet:27600]
Tarry stools [Orphanet:27600]
Melaena [Orphanet:27600]
Melaena [MedDRA:10027141]
Blood clot excretion [MedDRA:10027141]
Melena [MedDRA:10027141]
Stool tarry [MedDRA:10027141]
Tarry stools [MedDRA:10027141]
Melena (less common) [OMIM:Melena (less common)]
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: "Melena" [OMIM:Melena]
OMIM: "Melena (less common)" [OMIM:Melena (less common)]
UMLS:C0474585 "melena" [HPO:0002249]
UMLS:C0474585 "Feces color: tarry" [Orphanet:27600]
UMLS:C0025222 "Melena" [Orphanet:27600]
UMLS:C0267596 "Rectal hemorrhage" [Orphanet:27600]
Is a (Direct Parents):
Orphanet Functional anomalies of the digestive system
MedDRA Gastrointestinal hemorrhage
HPO         Gastrointestinal hemorrhage
Orphanet 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)
                      Melena(HPO:0002249)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Internal hemorrhage(HPO:0011029)
                Gastrointestinal hemorrhage(HPO:0002239)
                   Melena(HPO:0002249)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Gastrointestinal hemorrhage(HPO:0002239)
                   Melena(HPO:0002249)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular haemorrhagic disorders(MedDRA:10047075)
       Gastrointestinal hemorrhage(HPO:0002239)
          Melena(HPO:0002249)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Lymphangioleiomyomatosis (Orphanet:538)
Menkes disease (Orphanet:565)
Neonatal hemochromatosis (Orphanet:446)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
Transaldolase deficiency (Orphanet:101028)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
Wolfram syndrome (Orphanet:3463)