Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital pancreatic cyst |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Congenital pancreatic enterokinase deficiency |
Is a |
False |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Pancreatic duct anomaly |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Ectopic pancreas |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Annular pancreas |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Congenital hypoplasia of pancreas |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Accessory pancreas |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Congenital absence of pancreas (disorder) |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Anomalies of pancreas |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
[X]Other congenital malformations of pancreas and pancreatic duct |
Is a |
False |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Pancreas divisum |
Is a |
False |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Shwachman syndrome |
Is a |
False |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Islet cell hyperplasia |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
hypogonadisme, diabète sucré, alopécie, arriération mentale et anomalies électrocardiographiques |
Is a |
False |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Megaloblastic anaemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Renal-hepatic-pancreatic dysplasia is a rare, genetic, developmental defect during embryogenesis syndrome characterized by the triad of pancreatic fibrosis (and cysts, with a reduction of parenchymal tissue), renal dysplasia (with peripheral cortical cysts, primitive collecting ducts, glomerular cysts and metaplastic cartilage) and hepatic dysgenesis (enlarged portal areas containing numerous elongated binary profiles with a tendency to perilobular fibrosis). Situs abnormalities, skeletal anomalies and anencephaly have also been associated. Patients that survive the neonatal period present renal insufficiency, chronic jaundice and insulin-dependent diabetes. |
Is a |
True |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|
Partial agenesis of the pancreas is characterized by the congenital absence of a critical mass of pancreatic tissue. |
Is a |
False |
Congenital malformation of pancreas |
Inferred relationship |
Some |
|