Pancreatitis
Symptom Information:
Symptom ID: | HPO:0001733 | |||||||||||
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 pancreas(HPO:0001732) Abnormality of pancreas physiology(HPO:0012091) Pancreatitis(HPO:0001733) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Exocrine pancreas conditions(MedDRA:10015674) Acute and chronic pancreatitis(MedDRA:10033646) Pancreatitis(HPO:0001733) |
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Database Frequency: | 46 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Behçet disease | (Orphanet:117) |
Benign recurrent intrahepatic cholestasis | (Orphanet:65682) |
Benign recurrent intrahepatic cholestasis type 1 | (Orphanet:99960) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Chylous ascites | (Orphanet:1160) |
Citrullinemia type II | (Orphanet:247585) |
Classic maple syrup urine disease | (Orphanet:268145) |
Classical homocystinuria | (Orphanet:394) |
Familial Mediterranean fever | (Orphanet:342) |
Familial apolipoprotein C-II deficiency | (Orphanet:309020) |
Familial hypocalciuric hypercalcemia | (Orphanet:405) |
Familial hypocalciuric hypercalcemia type 1 | (Orphanet:93372) |
Familial hypocalciuric hypercalcemia type 2 | (Orphanet:101049) |
Familial hypocalciuric hypercalcemia type 3 | (Orphanet:101050) |
Familial lipoprotein lipase deficiency | (Orphanet:309015) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Familial partial lipodystrophy, Köbberling type | (Orphanet:79084) |
Familial visceral myopathy | (Orphanet:2604) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hereditary chronic pancreatitis | (Orphanet:676) |
Intermittent maple syrup urine disease | (Orphanet:268173) |
Legionellosis | (Orphanet:549) |
Low phospholipid associated cholelithiasis | (Orphanet:69663) |
Lyell syndrome | (Orphanet:537) |
Lysinuric protein intolerance | (Orphanet:470) |
MELAS | (Orphanet:550) |
Microscopic polyangiitis | (Orphanet:727) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX | (OMIM:260480) |
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME | (OMIM:606721) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Polyarteritis nodosa | (Orphanet:767) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary lipodystrophy | (Orphanet:90970) |
Propionic acidemia | (Orphanet:35) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Systemic capillary leak syndrome | (Orphanet:188) |
Thiamine-responsive maple syrup urine disease | (Orphanet:268184) |
Vitamin B12-unresponsive methylmalonic acidemia | (Orphanet:27) |
Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
Vitamin B12-unresponsive methylmalonic acidemia type mut0 | (Orphanet:289916) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |