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Results: 8

1.

Cirrhosis

MedGen UID:
351476
Concept ID:
C1623038
Disease or Syndrome
2.

Peritonitis

INFLAMMATION of the PERITONEUM lining the ABDOMINAL CAVITY as the result of infectious, autoimmune, or chemical processes. Primary peritonitis is due to infection of the PERITONEAL CAVITY via hematogenous or lymphatic spread and without intra-abdominal source. Secondary peritonitis arises from the ABDOMINAL CAVITY itself through RUPTURE or ABSCESS of intra-abdominal organs. [from MeSH]

MedGen UID:
14697
Concept ID:
C0031154
Disease or Syndrome
3.

Ascites

A disorder characterized by accumulation of serous or hemorrhagic fluid in the peritoneal cavity. [from NCI]

MedGen UID:
416
Concept ID:
C0003962
Disease or Syndrome
4.

Bacterial peritonitis

MedGen UID:
574434
Concept ID:
C0341503
Disease or Syndrome
5.

Peritonitis

`Inflammation` (MPATH:212) of the `peritoneum` (FMA:9584). [from HPO]

MedGen UID:
505282
Concept ID:
CN002348
Finding
6.

Cirrhosis

A chronic disorder of the `liver` (FMA:7197) in which liver tissue becomes `scarred` (PATO:0001850) and is partially replaced by regenerative nodules and fibrotic tissue resulting in loss of liver function. [from HPO]

MedGen UID:
504826
Concept ID:
CN001275
Finding
7.

Proton Pump Inhibitors

Any one of the substituted benzimidazole compounds with anti-ulcer activity. A proton pump inhibitor is orally administered in the neutrally charged, inactive form and, upon entering the acidic environment of the parietal cell, gets protonated and converted into its active form. The active form will covalently and irreversibly bind to the proton pump, the H+/K+-ATPase, located on the surface of parietal cells. This leads to an inhibition of the transport of hydrogen ions, in exchange for potassium ions, into the gastric lumen and results in an inhibition of gastric acid secretion. [from NCI]

MedGen UID:
87634
Concept ID:
C0358591
Pharmacologic Substance
8.

Cirrhosis of liver

Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. [from MeSH]

MedGen UID:
7368
Concept ID:
C0023890
Disease or Syndrome

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