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Items: 1 to 20 of 22

1.

Atherosclerosis

A condition characterized by patchy atheromas or atherosclerotic plaques which develop in the walls of medium-sized and large arteries and can lead to arterial stenosis with reduced or blocked blood flow. [from HPO]

MedGen UID:
13948
Concept ID:
C0004153
Disease or Syndrome
2.

Atherogenesis

MedGen UID:
327644
Concept ID:
C1563937
Pathologic Function
3.

Hereditary diffuse leukoencephalopathy with spheroids

MedGen UID:
777989
Concept ID:
C3711381
Disease or Syndrome
4.

Hypobetalipoproteinemia

An decreased concentration of low-density lipoprotein cholesterol in the blood. [from HPO]

MedGen UID:
776554
Concept ID:
C0853085
Finding
5.

Decreasing

MedGen UID:
617794
Concept ID:
C0442797
Finding
6.

Hereditary diffuse leukoencephalopathy with spheroids

CSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is characterized by executive dysfunction, memory decline, personality changes, motor impairments, and seizures. A frontal lobe syndrome (e.g., loss of judgment, lack of social inhibitors, lack of insight, and motor persistence) usually appears early in the disease course. The mean age of onset is usually in the fourth decade. Affected individuals eventually become bedridden with spasticity and rigidity. The disease course ranges from two to 30 or more years (mean: 8 years). [from GTR]

MedGen UID:
341741
Concept ID:
C1857300
7.

Hyperalphalipoproteinemia

An autosomal dominant genetic condition caused by mutation(s) in the CETP gene, encoding cholesteryl ester transfer protein. Affected individuals may have increased longevity due to decreased risk of coronary heart disease. [from NCI]

MedGen UID:
87465
Concept ID:
C0342883
Disease or Syndrome
8.

Heart disease

A non-neoplastic or neoplastic disorder that affects the heart and/or the pericardium. Representative examples include endocarditis, pericarditis, atrial myxoma, cardiac myeloid sarcoma, and pericardial malignant mesothelioma. [from NCI]

MedGen UID:
5458
Concept ID:
C0018799
Disease or Syndrome
9.

Coronary heart disease

An imbalance between myocardial functional requirements and the capacity of the CORONARY VESSELS to supply sufficient blood flow. It is a form of MYOCARDIAL ISCHEMIA (insufficient blood supply to the heart muscle) caused by a decreased capacity of the coronary vessels. [from MeSH]

MedGen UID:
3624
Concept ID:
C0010068
Disease or Syndrome
10.

Inborn genetic diseases

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. [from MeSH]

MedGen UID:
181981
Concept ID:
C0950123
Disease or Syndrome
11.

Disorder of lipid metabolism

An inherited metabolic disorder caused by an enzyme deficiency, resulting in an inability to oxidize fatty acids for energy production. [from NCI]

MedGen UID:
57587
Concept ID:
C0154251
Disease or Syndrome
12.

Nutritional and Metabolic Diseases

A collective term for nutritional disorders resulting from poor absorption or nutritional imbalance, and metabolic disorders resulting from defects in biosynthesis (ANABOLISM) or breakdown (CATABOLISM) of endogenous substances. [from MeSH]

MedGen UID:
45164
Concept ID:
C0028715
Disease or Syndrome
13.

Metabolic disease

A congenital (due to inherited enzyme abnormality) or acquired (due to failure of a metabolic important organ) disorder resulting from an abnormal metabolic process. [from NCI]

MedGen UID:
44376
Concept ID:
C0025517
Disease or Syndrome
14.

Vascular disorder

A non-neoplastic or neoplastic disorder affecting the arteries, veins, or lymphatic vessels. Examples include vasculitis, thrombophlebitis, arteriosclerosis, lymphedema, hemangioma, and angiosarcoma. [from NCI]

MedGen UID:
22621
Concept ID:
C0042373
Disease or Syndrome
15.

Arterial occlusive disease

A narrowing of the peripheral arteries (i.e., of arteries other than thos that supply the heart and the brain). [from HPO]

MedGen UID:
13913
Concept ID:
C0003838
Disease or Syndrome
16.

Inborn error of metabolism

A group of disorders present at birth that involve genetic defects leading to disturbances in carbohydrate, lipid, lysosomal storage or amino acid metabolism in the body. [from NCI]

MedGen UID:
6323
Concept ID:
C0025521
Congenital Abnormality; Disease or Syndrome
17.

Lipid Metabolism, Inborn Errors

Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable. [from MeSH]

MedGen UID:
6106
Concept ID:
C0023772
Disease or Syndrome
18.

Epicholesterol

MedGen UID:
4089
Concept ID:
C0014487
Organic Chemical; Pharmacologic Substance
19.

Disorder of cardiovascular system

A non-neoplastic or neoplastic disorder affecting the heart or the vessels (arteries, veins and lymph vessels). Representative examples of non-neoplastic cardiovascular disorders are endocarditis and hypertension. Representative examples of neoplastic cardiovascular disorders are endocardial myxoma and angiosarcoma. [from NCI]

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

Arteriosclerosis

A vascular disorder characterized by thickening and hardening of the walls of the arteries. [from NCI]

MedGen UID:
2076
Concept ID:
C0003850
Disease or Syndrome
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