U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Search results

Items: 4

  • The following terms were not found in MedGen: 12674, PTA-12674.
1.

Hereditary factor XI deficiency disease

Factor XI deficiency is an autosomal bleeding disorder characterized by reduced levels of factor XI in plasma (less than 15 IU/dL). Bleeding occurs mainly after trauma or surgery. On the basis of the concordance or discordance of F11 antigen and activity, the disorder is classified into the more frequent cross-reactive negative (CRM-) and the rarer CRM positive (CRM+) (summary by Duga and Salomon, 2009). [from OMIM]

MedGen UID:
8770
Concept ID:
C0015523
Disease or Syndrome
2.

Persistent truncus arteriosus

Truncus arteriosus (TA) is a rare congenital cardiovascular anomaly characterized by a single arterial trunk arising from the heart by means of a single semilunar valve (<I>i.e.</I> truncal valve). Pulmonary arteries originate from the common arterial trunk distal to the coronary arteries and proximal to the first brachiocephalic branch of the aortic arch. TA typically overrides a large outlet ventricular septal defect (VSD). The intracardiac anatomy usually displays situs solitus and atrioventricular (AV) concordance. [from ORDO]

MedGen UID:
52867
Concept ID:
C0041207
Congenital Abnormality
3.

PR segment depression

A reduction in voltage of the PR segment below baseline. [from HPO]

MedGen UID:
1647462
Concept ID:
C4553254
Finding
4.

PR segment elevation

An increase in voltage of the PR segment above baseline. [from HPO]

MedGen UID:
1630951
Concept ID:
C2121436
Finding
Format

Send to:

Choose Destination

Supplemental Content

Find related data

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...