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Results: 1 to 20 of 35

1.

Sudden infant death syndrome

Sudden infant death syndrome (SIDS) is a diagnosis of exclusion which should be made only after a thorough autopsy without identification of a specific cause of death (Mage and Donner, 2004). Weese-Mayer et al. (2007) provided a detailed review of genetic factors that have been implicated in SIDS. The authors concluded that SIDS represents more than 1 entity and has a heterogeneous etiology most likely involving several different genetically controlled metabolic pathways. [from OMIM]

MedGen UID:
52548
Concept ID:
C0038644
Disease or Syndrome
2.

Syndrome

A set of symptoms or conditions that occur together and suggest the presence of a certain disease or an increased chance of developing the disease. [from NCI]

MedGen UID:
11688
Concept ID:
C0039082
Disease or Syndrome
3.

Death

Irreversible cessation of all bodily functions, manifested by absence of spontaneous breathing and total loss of cardiovascular and cerebral functions. [from MeSH]

MedGen UID:
3696
Concept ID:
C0011065
4.

Infant death

MedGen UID:
639821
Concept ID:
C0549159
Finding
5.

Sudden infant death

MedGen UID:
603675
Concept ID:
C0425045
Finding
6.

Channelopathies

A variety of neuromuscular conditions resulting from MUTATIONS in ION CHANNELS manifesting as episodes of EPILEPSY; HEADACHE DISORDERS; and DYSKINESIAS. [from MeSH]

MedGen UID:
328427
Concept ID:
C1720983
Disease or Syndrome
7.

Long QT syndrome

A ventricular arrhythmia characterized by syncopal episodes and a long QT interval, sometimes leading to sudden death due to paroxysmal ventricular arrhythmia. This arrhythmia is associated with a prolongation of repolarization following depolarization of the cardiac ventricles. The prolongation of the Q-T interval combined with torsades de pointes manifests as several different forms; some may be acquired or congenital; some may lead to serious arrhythmia and sudden cardiac death. (NCI) [from NCI]

MedGen UID:
44193
Concept ID:
C0023976
Disease or Syndrome
8.

Cause of Death

The circumstance or condition that results in the death of a living being. (NCI) [from NCI]

MedGen UID:
40147
Concept ID:
C0007465
Finding
9.

Nitric Oxide

name of an inorganic chemical [from CHV]

MedGen UID:
14378
Concept ID:
C0028128
Pharmacologic Substance
10.

Liquid

MedGen UID:
725915
Concept ID:
C1304698
Finding
11.

Prolonged QT interval

Increased time between the start of the Q wave and the end of the T wave as measured by the electrocardiogram (EKG). [from HPO]

MedGen UID:
500908
Concept ID:
CN001508
Finding
12.

Reading (datum presentation)

A datum that is presented to a user by a meter or similar instrument. [from NCI]

MedGen UID:
312545
Concept ID:
C1705179
Finding
13.

Nitric Oxide Synthase Inhibitor

A class of agents that inhibit nitric oxide synthases (NOS), enzymes which catalyze the production of nitric oxide (NO). The three known NOS isoforms (neuronal, endothelial and inducible) are all dimeric, bi-domain enzymes that contain iron protoporphyrin IX, flavin adenine dinucleotide, mononucleotide, and tetrahydrobiopterin as bound prosthetic groups. (NCI04) [from NCI]

MedGen UID:
237169
Concept ID:
C1373060
Pharmacologic Substance
14.

Mutant

An altered form of an individual, organism, population, or genetic character that differs from the corresponding wild type due to one or more alterations (mutations). [from NCI]

MedGen UID:
109303
Concept ID:
C0596988
Cell or Molecular Dysfunction
15.

Inhibition

MedGen UID:
5809
Concept ID:
C0021469
Molecular Function
16.

Molecular Mechanisms of Pharmacological Action

Pharmacological activities at the molecular level of DRUGS and other exogenous compounds that are used to treat DISEASES and affect normal BIOCHEMISTRY. [from MeSH]

MedGen UID:
226255
Concept ID:
C1258062
Molecular Function
17.

Cardiovascular Abnormalities

Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS. [from MeSH]

MedGen UID:
116727
Concept ID:
C0243050
Disease or Syndrome
18.

Pathologic Processes

The abnormal mechanisms and forms involved in the dysfunctions of tissues and organs. [from MeSH]

MedGen UID:
18325
Concept ID:
C0030660
Pathologic Function
19.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Diseases existing at birth and often before birth, or that develop during the first month of life (INFANT, NEWBORN, DISEASES), regardless of causation. Of these diseases, those characterized by structural deformities are termed CONGENITAL ABNORMALITIES. [from MeSH]

MedGen UID:
14319
Concept ID:
C0027612
Disease or Syndrome
20.

Enzyme Inhibitors

compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. [from CRISP]

MedGen UID:
8652
Concept ID:
C0014432
Pharmacologic Substance

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