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Results 1 - 5 of 5 for Fibrochondrogenesis 2
  1. Fibrochondrogenesis 
    ... disorder in the family. FBCG1 FBCG2 Fibrochondrogenesis-1 Fibrochondrogenesis-2 Genetic Testing Registry: Fibrochondrogenesis 1 Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/fibrochondrogenesis - Genetics
  2. COL11A2 gene 
    ... COL11A2 gene have been identified in people with fibrochondrogenesis type 2, a disorder of bone growth characterized by severe skeletal abnormalities and hearing loss. Infants with fibrochondrogenesis type 2 have a very narrow chest that prevents the ...
    https://medlineplus.gov/genetics/gene/col11a2 - Genetics
  3. COL11A1 gene 
    ... letter to the editor regarding the mechanism underlying fibrochondrogenesis. Gene. 2013 Oct 10;528(2):367-8. doi: 10.1016/j.gene.2013. ... F, Alshammari MJ, Alkuraya FS. Molecular pathogenesis of fibrochondrogenesis: is ... deficiency? Gene. 2012 Dec 15;511(2):480-1. doi: 10.1016/j.gene.2012. ...
    https://medlineplus.gov/genetics/gene/col11a1 - Genetics
  4. 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
  5. 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