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Results: 5

1.

Prader-Willi syndrome

Prader-Willi (PWS) syndrome is characterized by severe hypotonia and feeding difficulties in early infancy, followed in later infancy or early childhood by excessive eating and gradual development of morbid obesity (unless eating is externally controlled). Motor milestones and language development are delayed. All individuals have some degree of cognitive impairment. A distinctive behavioral phenotype (with temper tantrums, stubbornness, manipulative behavior, and obsessive-compulsive characteristics) is common. Hypogonadism is present in both males and females and manifests as genital hypoplasia, incomplete pubertal development, and, in most, infertility. Short stature is common; characteristic facial features, strabismus, and scoliosis are often present, and non-insulin-dependent diabetes mellitus often occurs in obese individuals. [from GeneReviews]

MedGen UID:
46057
Concept ID:
C0032897
Congenital Abnormality
2.

modafinil

A drug that is being studied as a treatment for fatigue in patients with cancer. It belongs to the family of drugs called stimulants. [from NCI]

MedGen UID:
32669
Concept ID:
C0066677
Pharmacologic Substance
3.

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
4.

Excessive daytime sleepiness

MedGen UID:
505150
Concept ID:
CN001985
Finding
5.

Drowsiness

The sensation of struggling to remain awake. [from NCI]

MedGen UID:
4390
Concept ID:
C0013144
Finding

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