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Results 1 - 5 of 5 for Robinow syndrome
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  1. ROR2 gene 
    ... found to cause the autosomal recessive form of Robinow syndrome, a condition that affects the development of many ... changes lead to the skeletal abnormalities characteristic of Robinow syndrome. A lack of this protein during early development ...
    https://medlineplus.gov/genetics/gene/ror2 - Genetics
  2. DVL1 gene 
    ... found to cause the autosomal dominant form of Robinow syndrome, a condition that affects the development of many ... mutations underlie a variant type of autosomal dominant Robinow syndrome called the osteosclerotic form, which features increased bone ...
    https://medlineplus.gov/genetics/gene/dvl1 - Genetics
  3. WNT5A gene 
    ... found to cause the autosomal dominant form of Robinow syndrome, a condition that affects the development of many ... organs and tissues, leading to the features of Robinow syndrome. More About This Health Condition hWNT5A wingless-type ...
    https://medlineplus.gov/genetics/gene/wnt5a - Genetics
  4. FZD2 gene 
    ... gene have been found to cause autosomal dominant Robinow syndrome, a condition that affects the development of many ... it actually represents a subtype of autosomal dominant Robinow syndrome.Three of the known mutations change a single ...
    https://medlineplus.gov/genetics/gene/fzd2 - Genetics
  5. DVL3 gene 
    ... found to cause the autosomal dominant form of Robinow syndrome, a condition that affects the development of many ... many organs and tissues before birth, leading to Robinow syndrome. More About This Health Condition dishevelled 3 (homologous ...
    https://medlineplus.gov/genetics/gene/dvl3 - Genetics