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Results 1 - 10 of 35 for Lynch syndrome
  1. MSH6 gene 
    ... variants, one from each parent, while people with Lynch syndrome (described below) have a variant in one copy ... reported in about 13 percent of families with Lynch syndrome that have an identified gene variant. Lynch syndrome ...
    https://medlineplus.gov/genetics/gene/msh6 - Genetics
  2. PMS2 gene 
    ... variants, one from each parent, while people with Lynch syndrome (described below) have a variant in one copy ... reported in about 6 percent of families with Lynch syndrome that have an identified gene alteration. Lynch syndrome ...
    https://medlineplus.gov/genetics/gene/pms2 - Genetics
  3. MSH2 gene 
    ... variants , one from each parent, while people with Lynch syndrome (described below) have a variant in one copy ... Condition About 20 percent of all cases of Lynch syndrome with an identified gene variant are associated with ...
    https://medlineplus.gov/genetics/gene/msh2 - Genetics
  4. MLH1 gene 
    ... variants, one from each parent, while people with Lynch syndrome (described below) have a variant in one copy ... Condition About 40 percent of all cases of Lynch syndrome with an identified gene alteration are associated with ...
    https://medlineplus.gov/genetics/gene/mlh1 - Genetics
  5. EPCAM gene 
    ... mutations) in the EPCAM gene are associated with Lynch syndrome, a condition that increases the risk of developing ... variants account for up to 3 percent of Lynch syndrome cases. On chromosome 2, the EPCAM gene lies ...
    https://medlineplus.gov/genetics/gene/epcam - Genetics
  6. BRCA1 gene 
    ... clinical features and counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome. Obstet Gynecol ...
    https://medlineplus.gov/genetics/gene/brca1 - Genetics
  7. BRCA2 gene 
    ... clinical features and counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome. Obstet Gynecol ...
    https://medlineplus.gov/genetics/gene/brca2 - Genetics
  8. GBE1 gene 
    ... on PubMed Klein CJ, Boes CJ, Chapin JE, Lynch CD, Campeau NG, Dyck PJ, Dyck PJ. Adult polyglucosan body disease: case description of an expanding genetic and clinical syndrome. Muscle Nerve. 2004 Feb;29(2):323-8. ...
    https://medlineplus.gov/genetics/gene/gbe1 - Genetics
  9. COMT gene 
    ... 020. Citation on PubMed Bearden CE, Jawad AF, Lynch DR, ... in the 22q11.2 Deletion Syndrome. Child Neuropsychol. 2005 Feb;11(1):109-17. ...
    https://medlineplus.gov/genetics/gene/comt - Genetics
  10. CDH1 gene 
    ... Pennell E, MacMillan A, Fernandez B, Keller G, Lynch H, Shah SP, Guilford P, Gallinger S, Corso G, Roviello F, Caldas C, Oliveira C, Pharoah PD, Huntsman DG. Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. JAMA Oncol. 2015 Apr; ...
    https://medlineplus.gov/genetics/gene/cdh1 - Genetics
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