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Results 1 - 6 of 6 for Feingold syndrome 2
  1. MIR17HG gene 
    ... Repnikova EA, Amudhavalli SM. Expanding the phenotype of feingold syndrome-2. Am J Med Genet A. 2015 Dec;167A( ...
    https://medlineplus.gov/genetics/gene/mir17hg - Genetics
  2. IRF6 gene 
    ... IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet. 2002 Oct;32(2):285-9. doi: 10.1038/ng985. Epub 2002 Sep 3. Citation on PubMed or Free article on PubMed Central Mukhopadhyay N, Feingold E, Moreno-Uribe L, Wehby G, Valencia-Ramirez ...
    https://medlineplus.gov/genetics/gene/irf6 - Genetics
  3. MYCN gene 
    ... the MYCN gene have been found to cause Feingold syndrome type 1. This developmental disorder is characterized by ... for making the protein. In some cases of Feingold syndrome type 1, the entire MYCN gene is deleted. ...
    https://medlineplus.gov/genetics/gene/mycn - Genetics
  4. ORC6 gene 
    ... cells separate from one another (cytokinesis). At least two mutations in the ORC6 gene have been found ... origin recognition complex formation. Elife. 2013 Oct 8;2:e00882. doi: 10.7554/eLife.00882. Citation on ...
    https://medlineplus.gov/genetics/gene/orc6 - Genetics
  5. LORICRIN gene 
    ... give the stratum corneum its strength. At least two mutations in the LORICRIN gene have been identified ... Hachem JP, Behne M, Moskowitz DG, Christiano AM, Feingold KR, Elias PM. ... (Vohwinkel syndrome with ichthyosis). J Invest Dermatol. 2004 Apr;122( ...
    https://medlineplus.gov/genetics/gene/loricrin - Genetics
  6. HOXA13 gene 
    ... foot-genital syndrome. Nat Genet. 1997 Feb;15(2):179-80. doi: 10.1038/ng0297-179. Citation ...
    https://medlineplus.gov/genetics/gene/hoxa13 - Genetics