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Items: 1 to 20 of 37

1.

History

The aggregate of past events; the continuum of events occurring in succession leading from the past to the present; a record or narrative description of past events. [from NCI]

MedGen UID:
389153
Concept ID:
C2004062
Finding
2.

Fetal hydantoin syndrome

A teratogenic disorder observed in a newborn or child of a mother who was exposed to phenytoin during pregnancy. Manifestations include dysmorphic craniofacial features, hypoplastic distal phalanges and nails, growth delay and delayed psychomotor development.(NICHD) [from NCI]

MedGen UID:
75569
Concept ID:
C0265372
Disease or Syndrome
3.

Family history

MedGen UID:
69143
Concept ID:
C0241889
Finding
4.

Hypertension

MedGen UID:
6969
Concept ID:
C0020538
Disease or Syndrome
5.

Asthma

MedGen UID:
2109
Concept ID:
C0004096
Disease or Syndrome
6.

CHD

MedGen UID:
893225
Concept ID:
CN238725
Finding
7.

Bronchomoniliasis

MedGen UID:
737485
Concept ID:
C1622369
Disease or Syndrome
8.

Cheese-makers asthma

MedGen UID:
729880
Concept ID:
C1321272
Disease or Syndrome
9.

Hypertension

MedGen UID:
635666
Concept ID:
C0497247
Finding
10.

Meat-wrappers asthma

MedGen UID:
536788
Concept ID:
C0238266
Disease or Syndrome
11.

Asthma

MedGen UID:
505101
Concept ID:
CN001900
Finding
12.

Abnormality of the cardiovascular system

MedGen UID:
116727
Concept ID:
C0243050
Congenital Abnormality
13.

Generalized

Affecting all regions without specificity of distribution. [from HPO]

MedGen UID:
104661
Concept ID:
C0205246
Spatial Concept
14.

Chronic

Slow, creeping onset, slow progress and long continuance of disease manifestations. [from HPO]

MedGen UID:
104657
Concept ID:
C0205191
Temporal Concept
15.

History of

A record of a patient's background regarding health and the occurrence of disease events of the individual. In addition, personal medical history may be a variable in epidemiologic studies. [from NCI]

MedGen UID:
82657
Concept ID:
C0262926
Finding
16.

Congenital heart disease

Critical congenital heart disease (CCHD) is a term that refers to a group of serious heart defects that are present from birth. These abnormalities result from problems with the formation of one or more parts of the heart during the early stages of embryonic development. CCHD prevents the heart from pumping blood effectively or reduces the amount of oxygen in the blood. As a result, organs and tissues throughout the body do not receive enough oxygen, which can lead to organ damage and life-threatening complications. Individuals with CCHD usually require surgery soon after birth.Although babies with CCHD may appear healthy for the first few hours or days of life, signs and symptoms soon become apparent. These can include an abnormal heart sound during a heartbeat (heart murmur), rapid breathing (tachypnea), low blood pressure (hypotension), low levels of oxygen in the blood (hypoxemia), and a blue or purple tint to the skin caused by a shortage of oxygen (cyanosis). If untreated, CCHD can lead to shock, coma, and death. However, most people with CCHD now survive past infancy due to improvements in early detection, diagnosis, and treatment.Some people with treated CCHD have few related health problems later in life. However, long-term effects of CCHD can include delayed development and reduced stamina during exercise. Adults with these heart defects have an increased risk of abnormal heart rhythms, heart failure, sudden cardiac arrest, stroke, and premature death.Each of the heart defects associated with CCHD affects the flow of blood into, out of, or through the heart. Some of the heart defects involve structures within the heart itself, such as the two lower chambers of the heart (the ventricles) or the valves that control blood flow through the heart. Others affect the structure of the large blood vessels leading into and out of the heart (including the aorta and pulmonary artery). Still others involve a combination of these structural abnormalities.People with CCHD have one or more specific heart defects. The heart defects classified as CCHD include coarctation of the aorta, double-outlet right ventricle, D-transposition of the great arteries, Ebstein anomaly, hypoplastic left heart syndrome, interrupted aortic arch, pulmonary atresia with intact septum, single ventricle, total anomalous pulmonary venous connection, tetralogy of Fallot, tricuspid atresia, and truncus arteriosus.
[from GHR]

MedGen UID:
57501
Concept ID:
C0152021
Congenital Abnormality
17.

Heart disease

MedGen UID:
5458
Concept ID:
C0018799
Disease or Syndrome
18.

Coronary heart disease

MedGen UID:
3624
Concept ID:
C0010068
Disease or Syndrome
19.

Disorder of cardiovascular system

MedGen UID:
2848
Concept ID:
C0007222
Disease or Syndrome
20.

Disorder of glucose metabolism

A metabolic disorder characterized by abnormal blood glucose levels. [from NCI]

MedGen UID:
226229
Concept ID:
C1257958
Disease or Syndrome
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