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Results: 1 to 20 of 51

1.

Partial trisomy

MedGen UID:
220961
Concept ID:
C1297882
Congenital Abnormality
2.

Trisomy

The possession of a third chromosome of any one type in an otherwise diploid cell. [from MeSH]

MedGen UID:
21702
Concept ID:
C0041107
Disease or Syndrome
3.

Obesity

Obesity means having too much body fat. It is different from being overweight, which means weighing too much. The weight may come from muscle, bone, fat, and/or body water. Both terms mean that a person's weight is greater than what's considered healthy for his or her height. . Obesity occurs over time when you eat more calories than you use. The balance between calories-in and calories-out differs for each person. Factors that might affect your weight include your genetic makeup, overeating, eating high-fat foods, and not being physically active. . Being obese increases your risk of diabetes, heart disease, stroke, arthritis, and some cancers. If you are obese, losing even 5 to 10 percent of your weight can delay or prevent some of these diseases. For example, that means losing 10 to 20 pounds if you weigh 200 pounds. NIH: National Institute of Diabetes and Digestive and Kidney Diseases.  [from MedlinePlus]

MedGen UID:
18127
Concept ID:
C0028754
Disease or Syndrome
4.

Error occurred: cannot get document summary

ID:
449670

5.

Chromosome 16q, trisomy

MedGen UID:
447668
Concept ID:
CN036363
Disease or Syndrome
6.

Obesity

MedGen UID:
368429
Concept ID:
C1963185
Finding
7.

Mass of body structure

In medicine, a lump in the body. It may be caused by the abnormal growth of cells, a cyst, hormonal changes, or an immune reaction. A mass may be benign (not cancer) or malignant (cancer). [from NCI]

MedGen UID:
108287
Concept ID:
C0577559
Finding
8.

Fat

The glyceryl esters of a fatty acid, or of a mixture of fatty acids. They are generally odorless, colorless, and tasteless if pure, but they may be flavored according to origin. Fats are insoluble in water, soluble in most organic solvents. They occur in animal and vegetable tissue and are generally obtained by boiling or by extraction under pressure. They are important in the diet (DIETARY FATS) as a source of energy. (Grant & Hackh's Chemical Dictionary, 5th ed) [from MeSH]

MedGen UID:
5132
Concept ID:
C0015677
Pharmacologic Substance
9.

Anisomastia

MedGen UID:
381317
Concept ID:
C1854013
Disease or Syndrome
10.

Female

A person who belongs to the sex that normally produces ova. The term is used to indicate biological sex distinctions, or cultural gender role distinctions, or both. (NCI) [from NCI_CDISC]

MedGen UID:
8807
Concept ID:
C0015780
Finding
11.

Intellectual functioning disability

A developmental disorder characterized by less than average intelligence and significant limitations in adaptive behavior with onset before the age of 18. [from NCI]

MedGen UID:
7544
Concept ID:
C0025362
Mental or Behavioral Dysfunction
12.

Error occurred: cannot get document summary

ID:
775793

13.

Does not

MedGen UID:
721427
Concept ID:
C1299585
Finding
14.

Detected

MedGen UID:
617726
Concept ID:
C0442726
Finding
15.

Moderate

Indicates the condition may result in noticable adverse adverse consequences but is unlikely to be life-threatening or cause permanent injury.  [from HL7]

MedGen UID:
525853
Concept ID:
C0205081
16.

Attention deficit hyperactivity disorder

Attention deficit hyperactivity disorder (ADHD) manifests at age 2-3 years or by first grade at the latest. The main symptoms are distractibility, impulsivity, hyperactivity, and often trouble organizing tasks and projects, difficulty going to sleep, and social problems from being aggressive, loud, or impatient. [from HPO]

MedGen UID:
506017
Concept ID:
CN006126
Finding
17.

Abnormal facial shape

An abnormal morphology (form) of the face or its components. [from HPO]

MedGen UID:
505048
Concept ID:
CN001810
Finding
18.

Hyperactivity

MedGen UID:
504585
Concept ID:
CN000708
Finding
19.

Attention deficit-hyperactivity disorder

MedGen UID:
426927
Concept ID:
CN033424
Disease or Syndrome
20.

Peroxisome Biogenesis Disorder, Complementation Group H

MedGen UID:
356488
Concept ID:
C1866260
Disease or Syndrome

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