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Results 1 - 5 of 5 for Fibrochondrogenesis 1
  1. Fibrochondrogenesis 
    ... of the disorder in the family. FBCG1 FBCG2 Fibrochondrogenesis-1 Fibrochondrogenesis-2 Genetic Testing Registry: Fibrochondrogenesis 1 Genetic Testing Registry: Fibrochondrogenesis 2 Fibrochondrogenesis National Organization ...
    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 by severe ... abnormalities, hearing loss, and vision loss. Infants with fibrochondrogenesis type 1 have a very narrow chest that prevents the ...
    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)  
    ... Achondroplasia is a genetic condition that affects about 1 in 15,000 to 1 in 40,000 people. It makes your arms ...
    https://medlineplus.gov/dwarfism.html - Health Topics