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Items: 17

1.

Pancreatitis

INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis. [from MeSH]

MedGen UID:
14586
Concept ID:
C0030305
Disease or Syndrome
2.

Chymotrypsin

A serine endopeptidase secreted by the pancreas as its zymogen, CHYMOTRYPSINOGEN and carried in the pancreatic juice to the duodenum where it is activated by TRYPSIN. It selectively cleaves aromatic amino acids on the carboxyl side. [from MeSH]

MedGen UID:
971
Concept ID:
C0008742
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
3.

Chronic pancreatitis

A chronic form of pancreatitis. [from HPO]

MedGen UID:
101753
Concept ID:
C0149521
Disease or Syndrome
4.

Alcohol-induced pancreatitis

Acute or chronic INFLAMMATION of the PANCREAS due to excessive ALCOHOL DRINKING. Alcoholic pancreatitis usually presents as an acute episode but it is a chronic progressive disease in alcoholics. [from MeSH]

MedGen UID:
84027
Concept ID:
C0376670
Disease or Syndrome
5.

Trypsin

A serine endopeptidase that is formed from TRYPSINOGEN in the pancreas. It is converted into its active form by ENTEROPEPTIDASE in the small intestine. It catalyzes hydrolysis of the carboxyl group of either arginine or lysine. EC 3.4.21.4. [from MeSH]

MedGen UID:
21715
Concept ID:
C0041236
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
6.

Abnormality of the liver

An abnormality of the liver. [from HPO]

MedGen UID:
893061
Concept ID:
C4021780
Anatomical Abnormality
7.

Tropical calcific pancreatitis

MedGen UID:
334069
Concept ID:
C1842402
Disease or Syndrome
8.

Hereditary pancreatitis

A disorder characterized by recurrent episodes of pancreatitis that start at a young age. It is caused by mutations in the PRSS1 or SPINK1 genes. Patients are at a high risk of developing pancreatic carcinoma. [from NCI]

MedGen UID:
116056
Concept ID:
C0238339
Disease or Syndrome
9.

Chronic

Slow, creeping onset, slow progress and long continuance of disease manifestations. [from HPO]

MedGen UID:
104657
Concept ID:
C0205191
Temporal Concept
10.

Alcoholic liver disease

A disorder caused by damage to the liver parenchyma due to alcohol consumption. It may present with an acute onset or follow a chronic course, leading to cirrhosis. [from NCI]

MedGen UID:
9793
Concept ID:
C0023896
Disease or Syndrome
11.

Alcohol-induced organic mental disorder

Disorders related to or resulting from abuse or mis-use of alcohol. [from MeSH]

MedGen UID:
68632
Concept ID:
C0236664
Mental or Behavioral Dysfunction
12.

Substance-Related Disorder

A category of psychiatric disorders which include disorders related to the taking of a drug of abuse (including alcohol, prescribed medications and recreational drugs). [from NCI]

MedGen UID:
66746
Concept ID:
C0236969
Mental or Behavioral Dysfunction
13.

Disorder caused by alcohol

Disorders stemming from the misuse and abuse of alcohol. [from MeSH]

MedGen UID:
65935
Concept ID:
C0236970
Disease or Syndrome
14.

Protease preparation

A class of enzymes that catalyze the hydrolysis of peptide bonds in the interior of a polypeptide chain or protein molecule. [from NCI]

MedGen UID:
45389
Concept ID:
C0030946
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
15.

Abnormality of the pancreas

A non-neoplastic or neoplastic disorder that affects the pancreas. Representative examples of non-neoplastic disorders include pancreatitis and pancreatic insufficiency. Representative examples of neoplastic disorders include cystadenomas, carcinomas, lymphomas, and neuroendocrine neoplasms. [from NCI]

MedGen UID:
14583
Concept ID:
C0030286
Disease or Syndrome
16.

Abnormality of the gastrointestinal tract

An abnormality of the gastrointestinal tract. [from HPO]

MedGen UID:
3828
Concept ID:
C0012242
Disease or Syndrome
17.

CTRC Gene Mutation

A change in the nucleotide sequence of the CTRC gene. [from NCI]

MedGen UID:
927383
Concept ID:
C4289851
Cell or Molecular Dysfunction
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