Steatorrhea

Symptom Information:

Symptom ID: HPO:0002570
Synonyms:
Fatty stool (finding) [Orphanet:27360]
STEATORRHOEA [HPO:0002570]
Steatorrhea [Orphanet:27360]
Steatorrhea [OMIM:Steatorrhea]
Malabsorption/chronic diarrhea/steatorrhea [Orphanet:27360]
Steatorrhoea [Orphanet:27360]
Steatorrhoea [MedDRA:10041969]
Fatty stools [MedDRA:10041969]
Pancreatic steatorrhea [MedDRA:10041969]
Pancreatic steatorrhoea [MedDRA:10041969]
Steatorrhea [MedDRA:10041969]
Quality:
Cross references:
Orphanet:27360 "Malabsorption/chronic diarrhea/steatorrhea" [Orphanet:27360]
OMIM: "Steatorrhea" [OMIM:Steatorrhea]
UMLS:C0038238 "STEATORRHOEA" [HPO:0002570]
UMLS:C0038238 "Steatorrhea" [Orphanet:27360]
Is a (Direct Parents):
MedDRA Malabsorption
HPO         Fat malabsorption
Orphanet Functional anomalies of the digestive system
Orphanet Malabsorption
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)
                Abnormality of the intestine(HPO:0002242)
                   Malabsorption(HPO:0002024)
                      Fat malabsorption(HPO:0002630)
                         Steatorrhea(HPO:0002570)
                   Abnormality of the small intestine(HPO:0002244)
                      Fat malabsorption(HPO:0002630)
                         Steatorrhea(HPO:0002570)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Malabsorption conditions(MedDRA:10025477)
       Malabsorption(HPO:0002024)
          Steatorrhea(HPO:0002570)
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
BILE ACID MALABSORPTION, PRIMARY (OMIM:613291)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CONGENITAL SHORT BOWEL SYNDROME (OMIM:615237)
Cholesteryl ester storage disease (Orphanet:75234)
Chylomicron retention disease (Orphanet:71)
Congenital bile acid synthesis defect type 1 (Orphanet:79301)
Congenital bile acid synthesis defect type 2 (Orphanet:79303)
Congenital bile acid synthesis defect type 3 (Orphanet:79302)
Cystinosis (Orphanet:213)
Familial hypercholanemia (Orphanet:238475)
Hereditary chronic pancreatitis (Orphanet:676)
Isolated sedoheptulokinase deficiency (ORPHA:440713)
Leprechaunism (Orphanet:508)
Lysosomal acid lipase deficiency (Orphanet:275761)
MELAS (Orphanet:550)
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY (OMIM:601347)
Maternally-inherited diabetes and deafness (Orphanet:225)
Maturity-onset diabetes of the young, type 8, with exocrine dysfunction (OMIM:609812)
Menkes disease (Orphanet:565)
NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET (OMIM:616263)
PANCREATIC AGENESIS 2 (OMIM:615935)
PEROXISOME BIOGENESIS DISORDER 3B (OMIM:266510)
Pancreatic insufficiency - anemia - hyperostosis (Orphanet:199337)
Pancreatic triacylglycerol lipase deficiency (Orphanet:309031)
Primary systemic amyloidosis (Orphanet:314701)
Reynolds syndrome (Orphanet:779)
Shwachman-Diamond syndrome (Orphanet:811)
Wolfram syndrome (Orphanet:3463)
Wolman disease (Orphanet:75233)