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Results 1 - 10 of 385 for Williams syndrome
  1. Williams syndrome 
    Williams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability ...
    https://medlineplus.gov/genetics/condition/williams-syndrome - Genetics
  2. Williams syndrome 
    Williams syndrome is a rare disorder that can lead to problems with development. ... Williams syndrome is caused by not having a copy of 25 to 27 genes on chromosome number 7. ...
    https://medlineplus.gov/ency/article/001116.htm - Medical Encyclopedia
  3. Williams Syndrome (For Parents) (Nemours Foundation)  
    Birth Defects/Specifics ... Birth Defects ... Congenital Heart Defects/Children ... Congenital Heart Defects ... Nemours Foundation ... Williams Syndrome, elastin arteriopathy, ...
    https://kidshealth.org/en/parents/williams-syndrome.html - External Health Links
  4. Williams Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Developmental Disabilities/Specifics ... Developmental Disabilities ... Genetic Disorders/Specifics ... Genetic Disorders ... Genetic and Rare Diseases Information Center ...
    https://rarediseases.info.nih.gov/diseases/7891/williams-syndrome - National Institutes of Health
  5. GTF2I gene 
    ... 7 that is missing (deleted) in people with Williams syndrome, which is a developmental disorder characterized by mild ... As a result of the deletion, people with Williams syndrome are missing one copy of the GTF2I gene ...
    https://medlineplus.gov/genetics/gene/gtf2i - Genetics
  6. LIMK1 gene 
    ... chromosome 7 that is deleted in people with Williams syndrome, which is a developmental disorder characterized by mild ... As a result of the deletion, people with Williams syndrome are missing one copy of the LIMK1 gene ...
    https://medlineplus.gov/genetics/gene/limk1 - Genetics
  7. GTF2IRD1 gene 
    ... chromosome 7 that is deleted in people with Williams syndrome, which is a developmental disorder characterized by mild ... As a result of the deletion, people with Williams syndrome are missing one copy of the GTF2IRD1 gene ...
    https://medlineplus.gov/genetics/gene/gtf2ird1 - Genetics
  8. CLIP2 gene 
    ... chromosome 7 that is deleted in people with Williams syndrome. As a result of this deletion, people with ... contribute to some of the characteristic features of Williams syndrome, including the unique behavioral traits and other symptoms ...
    https://medlineplus.gov/genetics/gene/clip2 - Genetics
  9. ELN gene 
    ... chromosome 7 that is deleted in people with Williams syndrome, which is a developmental disorder that is characterized ... As a result of the deletion, people with Williams syndrome are missing one copy of the ELN gene ...
    https://medlineplus.gov/genetics/gene/eln - Genetics
  10. Chromosome 7 
    ... WBSCR) because its deletion causes a disorder called Williams syndrome (described below), also known as Williams-Beuren syndrome. ... Beuren syndrome critical region at 7q11.23 causes Williams syndrome. Features of this condition include mild to moderate ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
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