Pancreatitis

Symptom Information:

Symptom ID: HPO:0001733
Synonyms:
Pancreatitis (disorder) [Orphanet:30880]
Pancreatitis [Orphanet:30880]
Pancreatitis [OMIM:Pancreatitis]
Pancreatitis [MedDRA:10033645]
Pancreatitis NOS [MedDRA:10033645]
Pancreatitis steroid-induced [MedDRA:10033645]
Pancreatitis aggravated [MedDRA:10033645]
Pancreatitis due to gallstones [MedDRA:10033645]
Pancreatitis due to biliary obstruction [MedDRA:10033645]
Mass forming pancreatitis [MedDRA:10033645]
Toxic pancreatitis [MedDRA:10033645]
Quality:
Cross references:
Orphanet:30880 "Pancreatitis" [Orphanet:30880]
OMIM: "Pancreatitis" [OMIM:Pancreatitis]
UMLS:C0030305 "Pancreatitis" [HPO:0001733]
UMLS:C0030305 "Pancreatitis" [Orphanet:30880]
Is a (Direct Parents):
MedDRA Acute and chronic pancreatitis
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)
                   Pancreatitis(HPO:0001733)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Exocrine pancreas conditions(MedDRA:10015674)
       Acute and chronic pancreatitis(MedDRA:10033646)
          Pancreatitis(HPO:0001733)
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)