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Results 1 - 3 of 3 for "Weissenbacher-Zweymuller" syndrome
  1. Weissenbacher-Zweymüller syndrome 
    Weissenbacher-Zweymüller syndrome is a condition that affects bone growth. It is characterized by skeletal abnormalities, hearing loss, and distinctive facial features. ...
    https://medlineplus.gov/.../weissenbacher-zweymuller-syndrome - Genetics
  2. COL11A2 gene 
    ... signs and symptoms are similar to those of Weissenbacher-Zweymüller syndrome (described below) and to a form of Stickler ... in the COL11A2 gene has been associated with Weissenbacher-Zweymüller syndrome, a disorder of bone growth characterized by skeletal ...
    https://medlineplus.gov/genetics/gene/col11a2 - Genetics
  3. Otospondylomegaepiphyseal dysplasia 
    ... condition significantly overlap those of two similar conditions, Weissenbacher-Zweymüller syndrome and Stickler syndrome type III. All of these ... Birk OS. COL11A2 mutation associated with autosomal recessive ... and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED). ...
    https://medlineplus.gov/.../otospondylomegaepiphyseal-dysplasia - Genetics