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Results 1 - 5 of 5 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
  4. Bone Diseases (National Library of Medicine)  
    Your bones help you move, give you shape and support your body. They are living tissues that rebuild constantly throughout your life. During childhood and ...
    https://medlineplus.gov/bonediseases.html - Health Topics
  5. Dwarfism (National Library of Medicine)  
    People with dwarfism have short stature. This means that their height is under 4' 10" as an adult. They are usually of normal intelligence. Dwarfism most often ...
    https://medlineplus.gov/dwarfism.html - Health Topics