Steatorrhea
Symptom Information:
Symptom ID: | HPO:0002570 | |||||||||||
Synonyms: |
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Quality: | ||||||||||||
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 abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Abnormality of the intestine(HPO:0002242) Abnormality of the small intestine(HPO:0002244) Fat malabsorption(HPO:0002630) Steatorrhea(HPO:0002570) Malabsorption(HPO:0002024) Fat malabsorption(HPO:0002630) Steatorrhea(HPO:0002570) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Malabsorption conditions(MedDRA:10025477) Malabsorption(HPO:0002024) Steatorrhea(HPO:0002570) |
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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) |