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Results 1 - 5 of 5 for Retinal dysplasia
  1. COL2A1 gene 
    ... sensitive tissue at the back of the eye (retinal detachment). This ocular type of ... called dysplasia of the proximal femoral epiphyses that are characterized ...
    https://medlineplus.gov/genetics/gene/col2a1 - Genetics
  2. WDR35 gene 
    ... tissue at the back of the eye (the retina). Cilia also play a role in the development ... most commonly mutated gene in people with cranioectodermal dysplasia; at least eight mutations in this gene have ...
    https://medlineplus.gov/genetics/gene/wdr35 - Genetics
  3. WDR19 gene 
    ... tissue at the back of the eye (the retina). Cilia also play a role in the development ... gene have been found in individuals with cranioectodermal dysplasia. This condition is characterized by an elongated head ( ...
    https://medlineplus.gov/genetics/gene/wdr19 - Genetics
  4. IFT122 gene 
    ... tissue at the back of the eye (the retina). Cilia also play a role in the development ... Mutations in the IFT122 gene can cause cranioectodermal dysplasia. This condition is characterized by an elongated head ( ...
    https://medlineplus.gov/genetics/gene/ift122 - Genetics
  5. IFT43 gene 
    ... tissue at the back of the eye (the retina). Cilia also play a role in the development ... IFT43 gene is a rare cause of cranioectodermal dysplasia. This condition is characterized by an elongated head ( ...
    https://medlineplus.gov/genetics/gene/ift43 - Genetics