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Results 1 - 10 of 18 for Zaki syndrome
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  1. Cyclic vomiting syndrome 
    ... 7010.2006.00040. Citation on PubMed Boles RG, Zaki EA, Lavenbarg T, Hejazi R, Foran P, Freeborn J, Trilokekar S, McCallum R. Are pediatric and adult-onset cyclic vomiting syndrome (CVS) biologically different conditions? Relationship of adult-onset ...
    https://medlineplus.gov/genetics/condition/cyclic-vomiting-syndrome - Genetics
  2. SLC30A10 gene 
    ... Singhi P, Aulakh R, Ribeiro RT, Barsottini OG, Zaki MS, Del Rosario ML, Dyack S, Price V, Rideout A, Gordon K, Wevers RA, Chong WK, Mills PB. Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused ...
    https://medlineplus.gov/genetics/gene/slc30a10 - Genetics
  3. Hypermanganesemia with dystonia 
    ... Singhi P, Aulakh R, Ribeiro RT, Barsottini OG, Zaki MS, Del Rosario ML, Dyack S, Price V, Rideout A, Gordon K, Wevers RA, Chong WK, Mills PB. Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused ...
    https://medlineplus.gov/.../hypermanganesemia-with-dystonia - Genetics
  4. Aicardi-Goutières syndrome 
    ... Soler D, Olivieri I, Orcesi S, Aglan MS, Zaki MS, Abdel-Salam GM, Vanderver A, Kisand K, Rozenberg F, Lebon P, Crow YJ. Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, ...
    https://medlineplus.gov/.../condition/aicardi-goutieres-syndrome - Genetics
  5. TREX1 gene 
    ... Soler D, Olivieri I, Orcesi S, Aglan MS, Zaki MS, Abdel-Salam GM, Vanderver A, Kisand K, Rozenberg F, Lebon P, Crow YJ. Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, ...
    https://medlineplus.gov/genetics/gene/trex1 - Genetics
  6. RNASEH2C gene 
    ... Soler D, Olivieri I, Orcesi S, Aglan MS, Zaki MS, Abdel-Salam GM, Vanderver A, Kisand K, Rozenberg F, Lebon P, Crow YJ. Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, ...
    https://medlineplus.gov/genetics/gene/rnaseh2c - Genetics
  7. SAMHD1 gene 
    ... Soler D, Olivieri I, Orcesi S, Aglan MS, Zaki MS, Abdel-Salam GM, Vanderver A, Kisand K, Rozenberg F, Lebon P, Crow YJ. Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, ...
    https://medlineplus.gov/genetics/gene/samhd1 - Genetics
  8. Adams-Oliver syndrome 
    ... Faqeih E, Ansari S, Horton K, Ashour A, Zaki MS, Al-Zahrani F, Cueto-Gonzalez AM, Abdel-Salam G, Temtamy S, Alkuraya FS. Mutations in EOGT confirm the genetic heterogeneity of autosomal-recessive Adams-Oliver syndrome. Am J Hum Genet. 2013 Apr 4;92( ...
    https://medlineplus.gov/genetics/condition/adams-oliver-syndrome - Genetics
  9. EOGT gene 
    ... Faqeih E, Ansari S, Horton K, Ashour A, Zaki MS, Al-Zahrani F, Cueto-Gonzalez AM, Abdel-Salam G, Temtamy S, Alkuraya FS. Mutations in EOGT confirm the genetic heterogeneity of autosomal-recessive Adams-Oliver syndrome. Am J Hum Genet. 2013 Apr 4;92( ...
    https://medlineplus.gov/genetics/gene/eogt - Genetics
  10. UNC80 deficiency 
    ... Birnbaum RY, Birk OS. UNC80 mutation causes a syndrome of hypotonia, severe ... Faqeih E, Alasmari A, Zaki MS, Gleeson JG, Alkuraya FS. Mutations in UNC80, ...
    https://medlineplus.gov/genetics/condition/unc80-deficiency - Genetics
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