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Items: 1 to 20 of 21

1.

Biomarkers, Pharmacological

Measurable biological parameters that serve for drug development, safety and dosing (DRUG MONITORING). [from MeSH]

MedGen UID:
408203
Concept ID:
C1955886
Pharmacologic Substance
2.

Eosinophilic esophagitis

Eosinophilic esophagitis (EOE) has an incidence of approximately 1 per 10,000 people. Symptoms include difficulty feeding, failure to thrive, vomiting, epigastric or chest pain, dysphagia, and food impaction. Individuals with EOE are predominantly young males with a high rate of atopic disease, and the diagnosis is made by endoscopy and biopsy findings of isolated eosinophils in the esophagus (summary by Rothenberg et al., 2010). Genetic Heterogeneity of Eosinophilic Esophagitis Eosinophilic esophagitis-1 (EOE1) is associated with variation at chromosome 7q11.2. Another locus (EOE2; 613412) has been been associated with variation in the TSLP gene (607003) on chromosome 5q22. [from GTR]

MedGen UID:
83318
Concept ID:
C0341106
Disease or Syndrome
3.

Eosinophilia

Abnormal increase of EOSINOPHILS in the blood, tissues or organs. [from MeSH]

MedGen UID:
41824
Concept ID:
C0014457
Disease or Syndrome
4.

Esophagitis

An acute or chronic inflammatory process affecting the esophageal wall. [from NCI]

MedGen UID:
4549
Concept ID:
C0014868
Disease or Syndrome
5.

Eosinophilic esophagitis

MedGen UID:
880804
Concept ID:
CN236360
Finding
6.

Absence

MedGen UID:
739164
Concept ID:
C1689985
Anatomical Abnormality
7.

Cavity

MedGen UID:
734294
Concept ID:
C1510420
Anatomical Abnormality
8.

Esophagitis, eosinophilic, 2

MedGen UID:
462029
Concept ID:
C3150679
Disease or Syndrome
9.

Infiltration

The process of the diffusion or accumulation in a tissue or cells of a substance not normal to it or in amounts above normal. (NCI) [from NCI]

MedGen UID:
83059
Concept ID:
C0332448
Pathologic Function
10.

Central

Applies to an abnormality that is located close to the median plane or midline of the body or of the referenced structure. [from HPO]

MedGen UID:
59958
Concept ID:
C0205099
Spatial Concept
11.

Mediator of inflammation

The endogenous compounds that mediate inflammation (AUTACOIDS) and related exogenous compounds including the synthetic prostaglandins (PROSTAGLANDINS, SYNTHETIC). [from MeSH]

MedGen UID:
66209
Concept ID:
C0243042
Pharmacologic Substance
12.

Serpin

A family of serine proteinase inhibitors which are similar in amino acid sequence and mechanism of inhibition, but differ in their specificity toward proteolytic enzymes. Some members of the serpin family may be substrates rather than inhibitors of SERINE ENDOPEPTIDASES. [from MeSH]

MedGen UID:
48634
Concept ID:
C0036764
Amino Acid, Peptide, or Protein; Biologically Active Substance; Pharmacologic Substance
13.

Gastrointestinal disease

A non-neoplastic or neoplastic disorder that affects the gastrointestinal tract, anus, liver, biliary system, and pancreas. [from NCI]

MedGen UID:
8970
Concept ID:
C0017178
Disease or Syndrome
14.

Gastroenteritis

An inflammatory disorder that affects the upper and lower gastrointestinal tract. Most commonly, this is attributed to viruses; however bacteria, parasites or adverse reactions can also be the culprit. Symptoms include acute diarrhea and vomiting. [from NCI]

MedGen UID:
8967
Concept ID:
C0017160
Disease or Syndrome
15.

Disorder of esophagus

A non-neoplastic or neoplastic disorder that affects the esophagus. Representative examples of non-neoplastic disorders include esophagitis and esophageal ulcer. Representative examples of neoplastic disorders include carcinomas, lymphomas, and melanomas. [from NCI]

MedGen UID:
8693
Concept ID:
C0014852
Disease or Syndrome
16.

White blood cell disorder

Disordered formation of various types of leukocytes or an abnormal accumulation or deficiency of these cells. [from MeSH]

MedGen UID:
7325
Concept ID:
C0023510
Disease or Syndrome
17.

Hemic and Lymphatic Diseases

Hematologic diseases and diseases of the lymphatic system collectively. Hemic diseases include disorders involving the formed elements (e.g., ERYTHROCYTE AGGREGATION, INTRAVASCULAR) and chemical components (e.g., BLOOD PROTEIN DISORDERS); lymphatic diseases include disorders relating to lymph, lymph nodes, and lymphocytes. [from MeSH]

MedGen UID:
6780
Concept ID:
C0018981
Disease or Syndrome
18.

Hematologic disease

An abnormality of the hematopoietic system. [from HPO]

MedGen UID:
5483
Concept ID:
C0018939
Disease or Syndrome
19.

Tropical pulmonary eosinophilia

MedGen UID:
4087
Concept ID:
C0014458
Disease or Syndrome
20.

No fatty infiltration seen

MedGen UID:
930064
Concept ID:
C4304395
Finding
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