Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 5 of 5 for "Prader-willi" syndrome
  1. Prader-Willi syndrome 
    Prader-Willi syndrome is a complex genetic condition that affects many parts of the body. In infancy, this condition is characterized by weak muscle tone (hypotonia), ...
    https://medlineplus.gov/genetics/condition/prader-willi-syndrome - Genetics
  2. Chromosome 15 
    ... in it are also involved in conditions called Prader-Willi syndrome and Angelman syndrome (described below). Individuals with a15q11. ... deafness-infertility syndrome. More About This Health Condition Prader-Willi syndrome is caused by a loss of active genes ...
    https://medlineplus.gov/genetics/chromosome/15 - Genetics
  3. OCA2 gene 
    ... OCA2 gene is often deleted in individuals with Prader-Willi syndrome. A loss of this gene does not cause intellectual disability and the other characteristic features of Prader-Willi syndrome; however, people with this condition who are missing ...
    https://medlineplus.gov/genetics/gene/oca2 - Genetics
  4. Angelman syndrome 
    ... ClinicalTrials.gov ANGELMAN SYNDROME; AS PubMed Buiting K. Prader-Willi syndrome and Angelman syndrome. Am J Med Genet C ...
    https://medlineplus.gov/genetics/condition/angelman-syndrome - Genetics
  5. What are genomic imprinting and uniparental disomy?: MedlinePlus Genetics 
    ... genomic imprinting. The most well-known conditions include Prader-Willi syndrome , which is characterized by uncontrolled eating and obesity, ...
    https://medlineplus.gov/.../understanding/inheritance/updimprinting - Genetics