Fat malabsorption
Symptom Information:
Symptom ID: | HPO:0002630 | ||||
Synonyms: |
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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) Malabsorption(HPO:0002024) Fat malabsorption(HPO:0002630) MedDRA: |
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Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Abetalipoproteinemia | (Orphanet:14) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
BILE ACID MALABSORPTION, PRIMARY | (OMIM:613291) |
Chylomicron retention disease | (Orphanet:71) |
Congenital bile acid synthesis defect type 4 | (Orphanet:79095) |
Deafness - small bowel diverticulosis - neuropathy | (Orphanet:3217) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
Progressive familial intrahepatic cholestasis type 2 | (Orphanet:79304) |
STORM SYNDROME | (OMIM:185069) |
WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS | (OMIM:278100) |