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Items: 13

1.

Unspecified encephalopathy

Encephalopathy is a term that means brain disease, damage, or malfunction. In general, encephalopathy is manifested by an altered mental state. [from HPO]

MedGen UID:
39314
Concept ID:
C0085584
Disease or Syndrome
2.

Spongiform encephalopathy

Encephalopathy that is characterized by tiny holes apparent by microscopy, often due to prion disease. [from NCI]

MedGen UID:
924126
Concept ID:
C4281802
Disease or Syndrome
3.

ph+++

MedGen UID:
623899
Concept ID:
C0450409
Finding
4.

ph++

MedGen UID:
623898
Concept ID:
C0450408
Finding
5.

ph+

MedGen UID:
623897
Concept ID:
C0450407
Finding
6.

Encephalopathy

MedGen UID:
368408
Concept ID:
C1963101
Finding
7.

disease transmission

Transmission of disease from one individual to another. [from PSY]

MedGen UID:
66979
Concept ID:
C0242781
Pathologic Function
8.

Pepsin A

Formed from pig pepsinogen by cleavage of one peptide bond. The enzyme is a single polypeptide chain and is inhibited by methyl 2-diaazoacetamidohexanoate. It cleaves peptides preferentially at the carbonyl linkages of phenylalanine or leucine and acts as the principal digestive enzyme of gastric juice. [from MeSH]

MedGen UID:
18365
Concept ID:
C0030909
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
9.

Skin tags

Cutaneous skin tags also known as acrochorda or fibroepithelial polyps are small benign tumours that may either form secondarily over time primarily in areas where the skin forms creases, such as the neck, armpit or groin or may also be present at birth, in which case they usually occur in the periauricular region. [from HPO]

MedGen UID:
11452
Concept ID:
C0037293
Neoplastic Process
10.

Gerstmann-Straussler-Scheinker syndrome

Genetic prion diseases generally manifest with cognitive difficulties, ataxia, and myoclonus (abrupt jerking movements of muscle groups and/or entire limbs). The order of appearance and/or predominance of these features and other associated neurologic and psychiatric findings vary. Familial Creutzfeldt-Jakob disease (fCJD), Gerstmann-Sträussler-Scheinker (GSS) syndrome, and fatal familial insomnia (FFI) represent the core phenotypes of genetic prion disease. Note: A fourth clinical phenotype, known as Huntington disease like-1 (HDL-1) has been proposed, but this is based on a single report, and the underlying pathologic features would categorize it as GSS. Although it is clear that these four subtypes display overlapping clinical and pathologic features, recognition of these phenotypes can be useful when providing affected individuals and their families with information about the expected clinical course. The age at onset ranges from the third to ninth decade of life. The course ranges from a few months to several years (typically 5-7 years; in rare instances, >10 years). [from GeneReviews]

MedGen UID:
4886
Concept ID:
C0017495
Disease or Syndrome
11.

Caseins

A mixture of related phosphoproteins occurring in milk and cheese. The group is characterized as one of the most nutritive milk proteins, containing all of the common amino acids and rich in the essential ones. [from MeSH]

MedGen UID:
794
Concept ID:
C0007332
Amino Acid, Peptide, or Protein; Pharmacologic Substance
12.

Endopeptidases

nonEC category which corresponds to EC 3.4.21, EC 3.4.22, EC 3.4.23, EC 3.4.24, and EC 3.4.99. [from CRISP]

MedGen UID:
45389
Concept ID:
C0030946
Amino Acid, Peptide, or Protein; Enzyme; Pharmacologic Substance
13.

PEPSINOGEN I--SECOND LOCUS

MedGen UID:
854671
Concept ID:
C3887963
Finding
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