Exocrine pancreatic insufficiency

Symptom Information:

Symptom ID: HPO:0001738
Synonyms:
Pancreatic insufficiency [HPO:0001738]
Pancreatic exocrine insufficiency [Orphanet:30770]
Exocrine pancreatic insufficiency (disorder) [Orphanet:30770]
Exocrine pancreatic insufficiency [Orphanet:30770]
Exocrine pancreatic insufficiency [OMIM:Exocrine pancreatic insufficiency]
Pancreatic insufficiency [OMIM:Pancreatic insufficiency]
Pancreatic failure/exocrine pancreas disease [Orphanet:30770]
Pancreatic insufficiency [MedDRA:10033628]
Quality:
Cross references:
Orphanet:30770 "Pancreatic failure/exocrine pancreas disease" [Orphanet:30770]
OMIM: "Exocrine pancreatic insufficiency" [OMIM:Exocrine pancreatic insufficiency]
OMIM: "Pancreatic insufficiency" [OMIM:Pancreatic insufficiency]
UMLS:C0267963 "Exocrine pancreatic insufficiency" [Orphanet:30770]
Is a (Direct Parents):
MedDRA Pancreatic disorders NEC
HPO         Abnormality of pancreas physiology
Orphanet Abnormality of pancreas morphology
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 pancreas(HPO:0001732)
                Abnormality of pancreas physiology(HPO:0012091)
                   Exocrine pancreatic insufficiency(HPO:0001738)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Exocrine pancreas conditions(MedDRA:10015674)
       Pancreatic disorders NEC(MedDRA:10027692)
          Exocrine pancreatic insufficiency(HPO:0001738)
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cystic fibrosis (Orphanet:586)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Cystinosis (Orphanet:213)
Hemochromatosis type 2 (Orphanet:79230)
Hereditary chronic pancreatitis (Orphanet:676)
Johanson-Blizzard syndrome (Orphanet:2315)
Kearns-Sayre syndrome (Orphanet:480)
Maturity-onset diabetes of the young, type 4 (OMIM:606392)
Maturity-onset diabetes of the young, type 7 (OMIM:610508)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE (OMIM:260450)
Pancreatic agenesis, congenital (OMIM:260370)
Pancreatic insufficiency - anemia - hyperostosis (Orphanet:199337)
Pearson syndrome (Orphanet:699)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Renal cysts and diabetes syndrome (Orphanet:93111)
Shwachman-Diamond syndrome (Orphanet:811)
Wolcott-Rallison syndrome (Orphanet:1667)