Exocrine pancreatic insufficiency
Symptom Information:
Symptom ID: | HPO:0001738 | ||||||||
Synonyms: |
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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 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) |
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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) |