Fat malabsorption

Symptom Information:

Symptom ID: HPO:0002630
Synonyms:
Fat malabsorption [OMIM:Fat malabsorption]
Quality:
Cross references:
OMIM: "Fat malabsorption" [OMIM:Fat malabsorption]
Is a (Direct Parents):
HPO         Malabsorption
HPO         Abnormality of the small intestine
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:
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)