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Results 1 - 3 of 3 for fibrochondrogenesis
  1. Fibrochondrogenesis 
    Fibrochondrogenesis is a very severe disorder of bone growth. Affected infants have a very narrow chest, which prevents the lungs from developing normally. Most infants ...
    https://medlineplus.gov/genetics/condition/fibrochondrogenesis - Genetics
  2. COL11A1 gene 
    ... COL11A1 gene have been identified in people with fibrochondrogenesis type 1, a disorder of bone growth characterized ... abnormalities, hearing loss, and vision loss. Infants with fibrochondrogenesis type 1 have a very narrow chest that ...
    https://medlineplus.gov/genetics/gene/col11a1 - Genetics
  3. COL11A2 gene 
    ... COL11A2 gene have been identified in people with fibrochondrogenesis type 2, a disorder of bone growth characterized ... severe skeletal abnormalities and hearing loss. Infants with fibrochondrogenesis type 2 have a very narrow chest that ...
    https://medlineplus.gov/genetics/gene/col11a2 - Genetics