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Results 1 - 10 of 35 for CK syndrome
  1. Klippel-Trenaunay syndrome 
    ... PubMed Kihiczak GG, Meine JG, Schwartz RA, Janniger CK. Klippel-Trenaunay syndrome: a multisystem disorder possibly resulting from a pathogenic ...
    https://medlineplus.gov/.../condition/klippel-trenaunay-syndrome - Genetics
  2. Larsen syndrome 
    ... Feb 29. Citation on PubMed Sajnani AK, Yiu CK, King NM. Larsen syndrome: a review of the literature and case report. ...
    https://medlineplus.gov/genetics/condition/larsen-syndrome - Genetics
  3. Myoclonic epilepsy with ragged-red fibers 
    ... HA, Munhoz RP, Muzzio JA, Scola RH, Kay CK, Raskin S, Werneck LC, Bruhn H. Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report. Mov Disord. 2008 Jun 15;23( ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  4. Noonan syndrome 
    ... SYNDROME 6; NS6 NOONAN SYNDROME 9; NS9 NOONAN SYNDROME 10; NS10 PubMed Chen PC, Yin J, Yu HW, Yuan T, Fernandez M, Yung CK, Trinh QM, Peltekova VD, Reid JG, Tworog-Dube ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  5. EPCAM gene 
    ... Hoenselaar E, Hendriks-Cornelissen SJ, Tsui WY, Kong CK, Brunner HG, van Kessel AG, Yuen ST, van Krieken JH, Leung SY, Hoogerbrugge N. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of ...
    https://medlineplus.gov/genetics/gene/epcam - Genetics
  6. Lynch syndrome 
    ... Hoenselaar E, Hendriks-Cornelissen SJ, Tsui WY, Kong CK, Brunner HG, van Kessel AG, Yuen ST, van Krieken JH, Leung SY, Hoogerbrugge N. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of ...
    https://medlineplus.gov/genetics/condition/lynch-syndrome - Genetics
  7. Megacystis-microcolon-intestinal hypoperistalsis syndrome 
    ... van IJcken WF, Slivano OJ, Burns AJ, Christie CK, de Mesy Bentley KL, Brooks AS, ... hypoperistalsis syndrome in humans and mice. Proc Natl Acad Sci ...
    https://medlineplus.gov/...colon-intestinal-hypoperistalsis-syndrome - Genetics
  8. Intestinal pseudo-obstruction 
    ... van IJcken WF, Slivano OJ, Burns AJ, Christie CK, de Mesy Bentley KL, Brooks AS, ... hypoperistalsis syndrome in humans and mice. Proc Natl Acad Sci ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics
  9. CDH23 gene 
    ... R, Madeo AC, Turriff A, Muskett JA, Zalewski CK, King KA, Ahmed ZM, Riazuddin S, ... or Usher syndrome USH1D in compound heterozygotes. J Med Genet. 2011 ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
  10. Pendred syndrome 
    ... PubMed Ito T, Choi BY, King KA, Zalewski CK, Muskett J, ... Pendred Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum ...
    https://medlineplus.gov/genetics/condition/pendred-syndrome - Genetics
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