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Results 1 - 10 of 32 for conversion disorder
  1. 17-beta hydroxysteroid dehydrogenase 3 deficiency 
    ... female sex hormone estrogen. Since impairment of the conversion to testosterone in this disorder results in excess androstenedione in the body, a ...
    https://medlineplus.gov/...hydroxysteroid-dehydrogenase-3-deficiency - Genetics
  2. Factor VII deficiency 
    ... Proconvertin deficiency Prothrombin conversion accelerator deficiency Serum prothrombin conversion accelerator deficiency ... PubMed Girolami ...
    https://medlineplus.gov/genetics/condition/factor-vii-deficiency - Genetics
  3. Campomelic dysplasia 
    ... homozygous nonsense mutation in SOX9 in the dominant disorder campomelic dysplasia: a case of mitotic gene conversion. Hum Genet. 2005 Jun;117(1):43-53. ...
    https://medlineplus.gov/genetics/condition/campomelic-dysplasia - Genetics
  4. Hypochondroplasia 
    ... of short-limbed dwarfism. This condition affects the conversion of cartilage into bone (a process called ossification), particularly in the long bones of the arms and legs. Hypochondroplasia is similar to another skeletal disorder called achondroplasia, but the features tend to be ...
    https://medlineplus.gov/genetics/condition/hypochondroplasia - Genetics
  5. Achondrogenesis 
    ... the normal development of cartilage and for its conversion to bone. ... several skeletal disorders that result from mutations in the COL2A1 gene. ...
    https://medlineplus.gov/genetics/condition/achondrogenesis - Genetics
  6. Bart-Pumphrey syndrome 
    ... growth and also impair hearing by disturbing the conversion of sound waves to nerve impulses. GJB2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases, an affected person has one ...
    https://medlineplus.gov/genetics/condition/bart-pumphrey-syndrome - Genetics
  7. Type 1 diabetes 
    ... is passed from the blood into cells for conversion to energy. Lack of insulin ... and symptoms of the disorder are caused by high blood glucose and may ...
    https://medlineplus.gov/genetics/condition/type-1-diabetes - Genetics
  8. Familial HDL deficiency 
    ... reduce the protein's ability to stimulate the conversion of cholesterol. These ABCA1 and APOA1 gene mutations decrease the ... Familial HDL deficiency is inherited in ...
    https://medlineplus.gov/genetics/condition/familial-hdl-deficiency - Genetics
  9. Diastrophic dysplasia 
    ... newborns. Diastrophic dysplasia is one of several skeletal disorders caused by mutations in the SLC26A2 gene. This gene provides instructions for making a protein that is essential for the normal development of cartilage and for its conversion to bone. Cartilage is a tough, flexible tissue ...
    https://medlineplus.gov/genetics/condition/diastrophic-dysplasia - Genetics
  10. Atelosteogenesis type 2 
    ... Atelosteogenesis type 2 is one of several skeletal disorders caused by mutations in the SLC26A2 gene. This gene provides instructions for making a protein that is essential for the normal development of cartilage and for its conversion to bone. Cartilage is a tough, flexible tissue ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-2 - Genetics
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